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GoTaq® qPCR and RT-qPCR Systems

PCR Satisfaction Guaranteed

Convenient Master Mixes for Quantitative Real-Time PCR and RT-qPCR

  • Ready-to-use mix of optimized components for dye-based qPCR or RT-qPCR
  • Compatible with both fast and standard cycling methods
  • Resistant to a wide range of PCR inhibitors

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$ 290.00
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GoTaq® qPCR and RT-qPCR Systems
qPCR/5ml
$ 290.00
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Simple, Sensitive, Dye-Based qPCR and RT-qPCR

The GoTaq® qPCR and RT-qPCR Systems are ready-to-use, 2X master mixes containing BRYT Green® Dye, a  fluorescent DNA binding dye with minimal PCR inhibition, providing maximum amplification efficiency and greater fluorescence enhancement than SYBR® Green I.

Rapid hot-start activation and processive enzymes make the  GoTaq® Systems compatible with most real-time PCR instruments using standard or fast cycling. The 1-Step and 2-Step RT-qPCR Systems also include GoScript™ Reverse Transcriptase, to enable efficient synthesis of first-strand cDNA in preparation for PCR.

Choose qPCR or RT-qPCR Master Mix Formats

GoTaq® qPCR Master Mix
GoTaq® 1-Step RT-qPCR System
GoTaq® 2-Step RT-qPCR System

Sensitivity and Specificity for qPCR

The GoTaq® qPCR Master Mix is a ready-to-use 2X master mix for real-time quantitative PCR. Combining GoTaq® Hot Start Polymerase, optimized buffer and the BRYT Green® Dye, the GoTaq® qPCR Master Mix provides robust real-time PCR with earlier quantification cycle values and broad-range detection. These qualities result in increased reliability, reproducibility and sensitivity for quantitative, real-time PCR.

Designed for use with any instrument capable of reading SYBR® Green I or FAM™ Dye, the GoTaq® qPCR Master Mix offers:

  • Sensitive detection for earlier quantitation of low- and high-copy targets.
  • Room-temperature setup,making it suitable for automation and high-throughput detection.
  • Compatibility with both fast and standard qPCR cycling methods.
Cat.#Size10µl Reactions20µl Reactions
A6001
5ml
1,000 reactions
500 reactions
A6002
25ml
5,000 reactions
2,500 reactions
A6001 SYBR Green & qPCR Master Mix Kit
qPCR with single-copy detection. The GAPDH gene was amplified and detected from 10-fold serial dilutions (0.01ng to 100ng) of human genomic DNA. Inset shows the standard curve for the various dilutions (Slope=-3.2; R2=0.995). Kit yield and purity were measured by absorbance spectroscopy.

Reverse Transcription and qPCR in One Reaction

The GoTaq® 1-Step RT-qPCR System enables detection and relative quantification of RNA expression levels using a one-step real-time RT-qPCR method, combining GoScript™ Reverse Transcriptase and GoTaq® qPCR Master Mix in a single reaction well. The GoScript™ RT Mix for 1-Step RT-qPCR (50X) combines optimized quantities amounts of GoScript™ Reverse Transcriptase, RNasin® Plus RNase Inhibitor and additives to enhance single-step reactions.

Other features provided by the 1-Step System include:

  • Sensitive detection for earlier quantitation of low- and high-copy-number targets over a broad dynamic range. Detects down to femtogram (fg) amounts of input RNA.
  • Exceptional room-temperature setup, allowing easy automation and high-throughput detection.
Cat.#Size10µl Reactions20µl Reactions
A6020
5ml
1,000 reactions
500 reactions
A6020 1-Step Real-Time PCR & qPCR Kit
Linear dynamic range from 100ng down to 10fg of human RNA template. Seven 10-fold dilutions of human total RNA was run using 200nM of each GAPDH transcript specific primer. The amplification curve shows 97% efficiency and an r2=0.999.

Two-Step Reverse Transcription and qPCR

The GoTaq® 2-Step RT-qPCR System facilitates detection and relative quantification of RNA expression levels via a two-step RT-qPCR method using GoScript™ Reverse Transcription System and GoTaq® qPCR Master Mix.

The GoTaq® qPCR Master Mix is provided as a ready-to-use, stabilized 2X formulation and contains GoTaq® Hot Start Polymerase, MgCl2, dNTPs, BRYT Green® Dye and a proprietary reaction buffer. This master mix contains a low level of carboxy-X-rhodamine (CXR); a separate tube of CXR reference dye is included.

The GoScript™ Reverse Transcription System includes an optimized reaction buffer and M-MLV reverse transcriptase designed to enable efficient synthesis of first-strand cDNA in preparation for PCR amplification. The cDNA product can be added directly to downstream qPCR amplification reactions.

 

Cat.#Size10µl Reactions20µl Reactions
A6010
5ml
50 × 20µl RT reactions
and 1,000 × 10µl
qPCR reactions
50 × 20µl RT reactions
and 500 × 20µl qPCR reactions
A6010 2-Step Real-Time PCR & qPCR Kit
Extended linear range. Dilutions of human reference total RNA were amplified with GoTaq® 2-Step RT-qPCR System looking at 5.8S expression. GoTaq® 2-Step system demonstrates a linear dynamic range over 9 orders of  magnitude with a high fluorescent signal. NTC reactions were all blank.

Performance Tested in qPCR with Many Sample Types and Instruments

We have generated experimental data using different systems, instruments, templates, samples and more. Just select the options below to narrow the selection.

 
131 out of 131 selected
DNA (10ng) from whole blood was amplified using the GoTaq® Probe qPCR Master Mix (Cat.# A6102) under both standard and Fast thermalcycling conditions on an ABI 7500 instrument. Equivalent Cq values were observed for RNaseP and APP regardless of cycling conditions used for the experiment.
Commercially available human K562 genomic DNA (Cat.#E4931) (10ng) was amplified using the GoTaq® Probe qPCR Master Mix (Cat.# A6102) under both standard and Fast thermalcycling conditions looking at RNaseP, TERT and APP. The three genes gave equivalent Cq values regardless of cycling conditions used for the experiment.
DNA (10ng) from a lung tumor FFPE sample was amplified using the GoTaq® Probe qPCR Master Mix (Cat.# A6102) under both standard and Fast thermalcycling conditions on an ABI 7500 instrument. Equivalent Cq values were observed for the three genes evaluated regardless of cycling conditions used for the experiment.
Gene expression levels for B2M, GNB2L1, and HPRT1 genes were determined via 1-Step RT-qPCR using 10ng of whole blood RNA with the GoTaq® 1-Step RT-qPCR System (Cat.# A6020) on an ABI 7500 using both standard and Fast thermalcycling conditions. Equivalent Cq values were observed for the three genes evaluated regardless of cycling conditions used for the experiment.
Gene expression levels for B2M, GNB2L1, and HPRT1 genes were determined via 1-Step RT-qPCR using 10ng of HCT116 cell RNA with the GoTaq®1-Step RT-qPCR System (Cat.# A6020) on an ABI 7500 using both standard and Fast thermalcycling conditions. Equivalent Cq values were observed for the three genes evaluated regardless of cycling conditions used for the experiment.
Gene expression levels for B2M, GNB2L1, and HPRT1 genes were determined via 1-Step RT-qPCR using 10ng of lung tumor FFPE RNA with the GoTaq® 1-Step RT-qPCR System (Cat.# A6020) on an ABI 7500 using both standard and Fast thermalcycling conditions. Equivalent Cq values were observed for the three genes evaluated regardless of cycling conditions used for the experiment.
Gene expression levels for B2M, GNB2L1, and HPRT1 genes were determined via 1-Step RT-qPCR using 10ng of whole blood RNA with the GoTaq® Probe 1-Step RT-qPCR System (Cat.# A6120) on an ABI 7500 using both standard and Fast thermalcycling conditions. Equivalent Cq values were observed for the three genes evaluated regardless of cycling conditions used for the experiment.
Gene expression levels for B2M, GNB2L1, and HPRT1 genes were determined via 1-Step RT-qPCR using 10ng of HCT116 cell RNA with the GoTaq® Probe 1-Step RT-qPCR System (Cat.# A6120) on an ABI 7500 using both standard and Fast thermalcycling conditions. Equivalent Cq values were observed for the three genes evaluated regardless of cycling conditions used for the experiment.
Gene expression levels for B2M, GNB2L1, and HPRT1 genes were determined via 1-Step RT-qPCR using 10ng of lung tumor FFPE RNA with the GoTaq® Probe 1-Step RT-qPCR System (Cat.# A6120) on an ABI 7500 using both standard and Fast thermalcycling conditions. Equivalent Cq values were observed for the three genes evaluated regardless of cycling conditions used for the experiment.
DNA (10ng) from whole blood was amplified using the GoTaq® qPCR Master Mix (Cat.# A6002) under both standard and Fast thermalcycling conditions on a BioRad CFX96 instrument. Equivalent Cq values were observed for all genes regardless of cycling conditions used for the experiment.
Commercially available human K562 genomic DNA (Cat.#E4931) (10ng) was amplified using the GoTaq® qPCR Master Mix (Cat.# A6002) under both standard and Fast thermalcycling conditions looking at RNaseP, TERT and APP on the Bio-Rad CFX96 qPCR instrument. The three genes gave equiavlent Cq values regardless of the thermalcycling conditions used for the experiment.
DNA (10ng) from a lung tissue FFPE sample was amplified using the GoTaq® qPCR Master Mix (Cat.# A6002) under both standard and Fast thermalcycling conditions on a BioRad CFX96 instrument. Equivalent Cq values were observed for all genes regardless of cycling conditions used for the experiment.
DNA (10ng) from whole blood was amplified using the GoTaq® Probe qPCR Master Mix (Cat.# A6102) under both standard and Fast thermalcycling conditions on a BioRad CFX96 instrument. Equivalent Cq values were observed for all genes regardless of cycling conditions used for the experiment.
Commercially available human K562 genomic DNA (Cat.#E4931) (10ng) was amplified using the GoTaq® Probe qPCR Master Mix (Cat.# A6102) under both standard and Fast thermalcycling conditions looking at RNaseP, TERT and APP on the Bio-Rad CFX96 qPCR instrument. The three genes gave equiavlent Cq values regardless of the thermalcycling conditions used for the experiment.
DNA (10ng) from a lung tissue FFPE sample was amplified using the GoTaq® Probe qPCR Master Mix (Cat.# A6102) under both standard and Fast thermalcycling conditions on a BioRad CFX96 instrument. Equivalent Cq values were observed for all genes regardless of cycling conditions used for the experiment.
Gene expression levels for B2M, GNB2L1, and HPRT1 genes were determined via 1-Step RT-qPCR using 10ng of whole blood RNA with the GoTaq® Probe 1-Step RT-qPCR System (Cat.# A6120) on a BioRad CFX96 instrument using both standard and Fast thermalcycling conditions. Equivalent Cq values were observed for the three genes evaluated regardless of cycling conditions used for the experiment.
Gene expression levels for B2M, GNB2L1, and HPRT1 genes were determined via 1-Step RT-qPCR using 10ng of HCT116 cell RNA with the GoTaq® Probe 1-Step RT-qPCR System (Cat.# A6120) on a BioRad CFX96 instrument using both standard and Fast thermalcycling conditions. Equivalent Cq values were observed for the three genes evaluated regardless of cycling conditions used for the experiment.
Gene expression levels for B2M, GNB2L1, and HPRT1 genes were determined via 1-Step RT-qPCR using 10ng of lung tumor FFPE RNA with the GoTaq® Probe 1-Step RT-qPCR System (Cat.# A6120) on a BioRad CFX96 instrument using both standard and Fast thermalcycling conditions. Equivalent Cq values were observed for the three genes evaluated regardless of cycling conditions used for the experiment.
DNA (10ng) from whole blood was amplified using the GoTaq® qPCR Master Mix (Cat.# A6002) under both standard and Fast thermalcycling conditions on a Roche Lightcycler 480 instrument using a 96 well plate. Equivalent Cq values were observed for all genes regardless of cycling conditions used for the experiment.
Commercially available human K562 genomic DNA (Cat.# E4931) (10ng) was amplified using the GoTaq® qPCR Master Mix (Cat.# A6002) under both standard and Fast thermalcycling conditions looking at RNaseP, TERT and APP on a Lightcycler 480 qPCR instrument using a 96 well plate. The three genes have equivalent Cq values reagrdless of the thermalcycing conditions used for the experiment.
DNA (10ng) from a lung tumor FFPE sample was amplified using the GoTaq® qPCR Master Mix (Cat.# A6002) under both standard and Fast thermalcycling conditions on a Roche Lightcycler 480 instrument using a 96 well plate. Equivalent Cq values were observed for the three genes evaluated regardless of cycling conditions used for the experiment.
DNA (10ng) from whole blood was amplified using the GoTaq® Probe qPCR Master Mix (Cat.# A6102) under both standard and Fast thermalcycling conditions on a Roche Lightcycler 480 instrument using a 96 well plate. RNaseP and APP had equivalent Cq values regardless of cycling conditions used for the experiment.
Commercially available human K562 genomic DNA (Cat.# E4931) (10ng) was amplified using the GoTaq® Probe qPCR Master Mix (Cat.# A6102) under both standard and Fast thermalcycling conditions looking at RNaseP, TERT and APP on a Lightcycler 480 qPCR instrument using a 96 well plate. The three genes have equivalent Cq values reagrdless of the thermalcycing conditions used for the experiment.
DNA (10ng) from a lung tumor FFPE sample was amplified using the GoTaq® Probe qPCR Master Mix (Cat.# A6102) under both standard and Fast thermalcycling conditions on a Roche Lightcycler 480 instrument using a 96 well plate. Equivalent Cq values were observed for the three genes evaluated regardless of cycling conditions used for the experiment.
Gene expression levels for B2M, GNB2L1, and HPRT1 genes were determined via 1-Step RT-qPCR using 10ng of whole blood RNA with the GoTaq® Probe 1-Step RT-qPCR System (Cat.# A6120) on a Roche Lightcycler 480 with a 96 well plate instrument using both standard and Fast thermalcycling conditions. Equivalent Cq values were observed for the three genes evaluated regardless of cycling conditions used for the experiment.
Gene expression levels for B2M, GNB2L1, and HPRT1 genes were determined via 1-Step RT-qPCR using 10ng of HCT116 cell RNA with the GoTaq® Probe 1-Step RT-qPCR System (Cat.# A6120) on a Roche Lightcycler 480 with a 96 well plate using both standard and Fast thermalcycling conditions. Equivalent Cq values were observed for the three genes evaluated regardless of cycling conditions used for the experiment.
Gene expression levels for B2M, GNB2L1, and HPRT1 genes were determined via 1-Step RT-qPCR using 10ng of lung tumor FFPE RNA with the GoTaq® Probe 1-Step RT-qPCR System (Cat.# A6120) on a Roche Lightcycler 480 instrument with a 96 well plate using both standard and Fast thermalcycling conditions. Equivalent Cq values were observed for the three genes evaluated regardless of cycling conditions used for the experiment.
DNA (10ng) from whole blood was amplified using the GoTaq® qPCR Master Mix (Cat.# A6002) under both standard and Fast thermalcycling conditions on a Roche Lightcycler 480 instrument using a 384 well plate. Equivalent Cq values were observed for RNaseP and APP regardless of cycling conditions used for the experiment.
Commercially available human K562 genomic DNA (Cat.# E4931) (10ng) was amplified using the GoTaq® qPCR Master Mix (Cat.# A6002) under both standard and Fast thermalcycling conditions looking at RNaseP, TERT and APP on a Lightcycler 480 qPCR instrument using a 384 well plate. RNaseP and APP gave equivalent Cq values regardless of the thermalcycling conditions used for the experiment.
DNA (10ng) from a lung tumor FFPE sample was amplified using the GoTaq® qPCR Master Mix (Cat.# A6002) under both standard and Fast thermalcycling conditions on a Roche Lightcycler 480 instrument with a 384 well plate. Equivalent Cq values were observed for RNaseP and APP evaluated regardless of cycling conditions used for the experiment.
DNA (10ng) from whole blood was amplified using the GoTaq(R) Probe qPCR Master Mix (Cat.# A6102) under both standard and Fast thermalcycling conditions on a Roche Lightcycler 480 instrument using a 384 well plate. Equivalent Cq values were observed for APP regardless of cycling conditions used for the experiment.
Commercially available human K562 genomic DNA (Cat.# E4931) (10ng) was amplified using the GoTaq® Probe qPCR Master Mix (Cat.# A6102) under both standard and Fast thermalcycling conditions looking at RNaseP, TERT and APP on a Lightcycler 480 qPCR instrument using a 384 well plate. APP samples showed equivalent Cq values regardless of the thermalcycling conditions used for the experiment.
DNA (10ng) from a lung tumor FFPE sample was amplified using the GoTaq® Probe qPCR Master Mix (Cat.# A6102) under both standard and Fast thermalcycling conditions on a Roche Lightcycler 480 instrument using a 384 well plate. Equivalent Cq values were observed for the three genes evaluated regardless of cycling conditions used for the experiment.
Gene expression levels for B2M, GNB2L1, and HPRT1 genes were determined via 1-Step RT-qPCR using 10ng of whole blood RNA with the GoTaq® Probe 1-Step RT-qPCR System (Cat.# A6120) on a Lightcycler 480 instrument with a 384 well plate using both standard and Fast thermalcycling conditions. Equivalent Cq values were observed for B2M and HPRT1 evaluated regardless of cycling conditions used for the experiment.
Gene expression levels for B2M, GNB2L1, and HPRT1 genes were determined via 1-Step RT-qPCR using 10ng of HCT116 cell RNA with the GoTaq® Probe 1-Step RT-qPCR System (Cat.# A6120) on a Roche Lightcycler 480 with a 384 well plate using both standard and Fast thermalcycling conditions.
Gene expression levels for B2M, GNB2L1, and HPRT1 genes were determined via 1-Step RT-qPCR using 10ng of lung tumor FFPE RNA with the GoTaq® Probe 1-Step RT-qPCR System (Cat.# A6120) on a Roche Lightcycler 480 with a 384 well plate using both standard and Fast thermalcycling conditions. Equivalent Cq values were observed for the three genes evaluated regardless of cycling conditions used for the experiment.
DNA (10ng) from whole blood was amplified using the GoTaq® qPCR Master Mix (Cat.# A6002) under both standard and Fast thermalcycling conditions on a Stratagene Mx3005P instrument looking at RNaseP, TERT and APP.
Commercially available human K562 genomic DNA (Cat.# E4931) (10ng) was amplified using the GoTaq® qPCR Master Mix (Cat.# A6002) under both standard and Fast thermalcycling condtions looking at RNaseP, TERT and APP on the Stratagene Mx3005P qPCR instrument.
DNA (10ng) from a lung tumor FFPE sample was amplified using the GoTaq® qPCR Master Mix (Cat.# A6002) under both standard and Fast thermalcycling conditions on a Stratagene Mx3005P instrument looking at RNaseP, TERT and APP.
DNA (10ng) from whole blood was amplified using the GoTaq® Probe qPCR Master Mix (Cat.# A6102) under both standard and Fast thermalcycling conditions on a Stratagene Mx3005P instrument looking at RNaseP and APP.
Commercially available human K562 genomic DNA (Cat.# E4931) (10ng) was amplified using the GoTaq® Probe qPCR Master Mix (Cat.# A6102) under both standard and Fast thermalcycling condtions looking at RNaseP, TERT and APP on the Stratagene Mx3005P qPCR instrument.
DNA (10ng) from a lung tumor FFPE sample was amplified using the GoTaq® Probe qPCR Master Mix (Cat.# A6102) under both standard and Fast thermalcycling conditions on a Stratagene Mx3005P instrument. Equivalent Cq values were observed for RNaseP and APP regardless of cycling conditions used for the experiment.
Gene expression levels for B2M, GNB2L1, and HPRT1 genes were determined via 1-Step RT-qPCR using 10ng of whole blood RNA with the GoTaq® 1-Step RT-qPCR System (Cat.# A6020) on a Stratagene Mx3005P using both standard and Fast thermalcycling conditions.
Gene expression levels for B2M, GNB2L1, and HPRT1 genes were determined via 1-Step RT-qPCR using 10ng of HCT116 cell RNA with the GoTaq® 1-Step RT-qPCR System (Cat.# A6020) on a Stratagene Mx3005P using both standard and Fast thermalcycling conditions.
Gene expression levels for B2M, GNB2L1, and HPRT1 genes were determined via 1-Step RT-qPCR using 10ng of lung tumor FFPE RNA with the GoTaq(R) 1-Step RT-qPCR System (Cat.# A6020) on a Stratagene Mx3005P using both standard and Fast thermalcycling conditions.
HCT116 cells were seeded at two different densities on GravityPLUS™ hanging drop 96-well plates (Insphero) to form microtissues. Purified RNA was evaluated via RT-qPCR using the GoTaq® Probe 1-Step RT-qPCR System (Cat. # A6120) looking at a high expressed gene, GNB2L1.
HCT116 cells were seeded at two different densities on GravityPLUS™ hanging drop 96-well plates (Insphero) to form microtissues. Purified RNA was evaluated via RT-qPCR using the GoTaq® Probe 1-Step RT-qPCR System (Cat. # A6120) looking at a low expressed gene, HPRT1.
HCT116 cells were seeded at two different densities on GravityPLUS™ hanging drop 96-well plates (Insphero) to form microtissues. Purified RNA was evaluated via RT-qPCR using the GoTaq® Probe 1-Step RT-qPCR System (Cat. # A6120) looking at a moderately expressed gene, B2M.
HCT116 cells were seeded at two different densities on GravityPLUS™ hanging drop 96-well plates (Insphero) to form microtissues. Purified RNA was evaluated by looking at the gene expression levels of three genes (GNB2L1, HPRT1, and B2M) using the GoTaq(R) Probe 1-Step RT-qPCR System (Cat. # A6120). The GoTaq(R) System was able to detect expression levels all three genes from RNA purified from two different microtissue densities.
HCT116 cells were seeded at two different densities on GravityPLUS™ hanging drop 96-well plates (Insphero) to form microtissues. Purified RNA was evaluated via RT-qPCR using the GoTaq® 1-Step RT-qPCR System (Cat. # A6020) looking at a high expressed gene, GNB2L1.
HCT116 cells were seeded at two different densities on GravityPLUS™ hanging drop 96-well plates (Insphero) to form microtissues. Purified RNA was evaluated via RT-qPCR using the GoTaq® 1-Step RT-qPCR System (Cat. # A6020) looking at a low expressed gene, HPRT1.
HCT116 cells were seeded at two different densities on GravityPLUS™ hanging drop 96-well plates (Insphero) to form microtissues. Purified RNA was evaluated via RT-qPCR using the GoTaq® 1-Step RT-qPCR System (Cat. # A6020) looking at a high expressed gene, B2M.
HCT116 cells were seeded at two different densities on GravityPLUS™ hanging drop 96-well plates (Insphero) to form microtissues. Purified RNA was evaluated by looking at the gene expression levels of three genes (GNB2L1, HPRT1, and B2M) using the GoTaq(R) 1-Step RT-qPCR System (Cat. # A6020). The GoTaq(R) System was able to detect all three genes from RNA purified from two different microtissue densities.
HCT116 cells were seeded at three different densities on GravityPLUS™ hanging drop 96-well plates (Insphero) to form microtissues. Purified gDNA was evaluted using the GoTaq(R) Probe qPCR Master Mix (Cat. # A6101) looking at the APP gene. The GoTaq(R) Probe Master Mix was able to detect APP from three different microtissue cell densities.
HCT116 cells were seeded at three different densities on GravityPLUS™ hanging drop 96-well plates (Insphero) to form microtissues. Purified gDNA was evaluted using the GoTaq(R) Probe qPCR Master Mix (Cat. # A6101) looking at the TERT gene. The GoTaq(R) Probe Master Mix was able to detect TERT from three different microtissue cell densities.
HCT116 cells were seeded at three different densities on GravityPLUS™ hanging drop 96-well plates (Insphero) to form microtissues. Purified gDNA was evaluted using the GoTaq(R) Probe qPCR Master Mix (Cat. # A6101) looking at the RNaseP gene. The GoTaq(R) Probe Master Mix was able to detect RNaseP from three different microtissue cell densities.
HCT116 cells were seeded at three different densities on GravityPLUS™ hanging drop 96-well plates (Insphero) to form microtissues. Purified gDNA was evaluated using the GoTaq(R) Probe qPCR Master Mix (Cat. # A6101). The GoTaq(R) Probe Master Mix was able to detect APP, TERT, and RNaseP from gDNA purified from three different microtissue densities.
HCT116 cells were seeded at three different densities on GravityPLUS™ hanging drop 96-well plates (Insphero) to form microtissues. Purified gDNA was evaluted using the GoTaq(R) qPCR Master Mix (Cat. # A6001) looking at the APP gene. The GoTaq(R) Master Mix was able to detect APP from three different microtissue cell densities.
HCT116 cells were seeded at three different densities on GravityPLUS™ hanging drop 96-well plates (Insphero) to form microtissues. Purified gDNA was evaluted using the GoTaq(R) qPCR Master Mix (Cat. # A6001) looking at the TERT gene. The GoTaq(R) Master Mix was able to detect TERT from three different microtissue cell densities.
HCT116 cells were seeded at three different densities on GravityPLUS™ hanging drop 96-well plates (Insphero) to form microtissues. Purified gDNA was evaluted using the GoTaq(R) qPCR Master Mix (Cat. # A6001) looking at the RNaseP gene. The GoTaq(R) Master Mix was able to detect RNaseP from three different microtissue cell densities.
HCT116 cells were seeded at three different densities on GravityPLUS™ hanging drop 96-well plates (Insphero) to form microtissues. Purified gDNA was evaluated using the GoTaq® qPCR Master Mix (Cat. # A6001). The GoTaq® Master Mix was able to detect APP, TERT, and RNaseP from gDNA purified from three different microtissue densities.
Circulating Cell Free DNA (CCF DNA) was purifed from plasma using the Maxwell® RSC instrument and Maxwell® RSC ccfDNA Plasma kit. Purified DNA was amplified using the GoTaq® Probe qPCR Master Mix (Cat. # A6101) looking at three genes, RNaseP, APP and TERT. The GoTaq(R) Probe qPCR Master Mix was able to amplify all three genes from purified ccfDNA.
Circulating Cell Free DNA (CCF DNA) was purifed from serum using the Maxwell® RSC instrument and Maxwell® RSC ccfDNA Plasma kit. Purified DNA was amplified using the GoTaq® Probe qPCR Master Mix (Cat. # A6101) looking at three genes, RNaseP, APP and TERT. The GoTaq(R) Probe qPCR Master Mix was able to amplify all three genes from purified ccfDNA.
Circulating Cell Free DNA (CCF DNA) was purifed from plasma using the Maxwell® RSC instrument and Maxwell® RSC ccfDNA Plasma kit. Purified DNA was amplified using the GoTaq® qPCR Master Mix (Cat. # A6001) looking at three genes, RNaseP, APP and TERT. The GoTaq(R) qPCR Master Mix was able to amplify all three genes from purified ccfDNA.
Circulating Cell Free DNA (CCF DNA) was purifed from serum using the Maxwell® RSC instrument and Maxwell® RSC ccfDNA Plasma kit. Purified DNA was amplified using the GoTaq® qPCR Master Mix (Cat. # A6001) looking at three genes, RNaseP, APP and TERT. The GoTaq(R) qPCR Master Mix was able to amplify all three genes from purified ccfDNA.
Four, tenfold dilutions of corn DNA were amplified via qPCR using the GoTaq® qPCR Master Mix (Cat.# A6001) looking at the cl3036_1 LOC100192652 gene.
Four, tenfold dilutions of soybean DNA were amplified via qPCR using the GoTaq® qPCR Master Mix (Cat.# A6001) looking at the ACPD gene.
Four, tenfold dilutions of Arabidopsis DNA were amplified via qPCR using the GoTaq® qPCR Master Mix (Cat.# A6001) looking at the AT302610 gene.
Expression levels for the EF1a gene in corn were evaluted via 1-step RT-qPCR using the GoTaq® 1-step RT-qPCR System (Cat. # A6020).
Expression levels for the Cons6 gene in soybean were evaluted via 1-step RT-qPCR using the GoTaq® 1-step RT-qPCR System (Cat. # A6020).
Expression levels for the EF1A gene in Arabidopsis were evaluted via 1-step RT-qPCR using the GoTaq® 1-step RT-qPCR System (Cat. # A6020).
Expression levels for the Zmm19 gene in corn were evaluted via 1-step RT-qPCR using the GoTaq® Probe 1-Step RT-qPCR System (Cat. # A6120).
Expression levels for the PEPC17 gene in soybean were evaluted via 1-step RT-qPCR using the GoTaq® Probe 1-Step RT-qPCR System (Cat. # A6120).
Expression levels for the NY-YB1 gene in Arabidopsis were evaluted via 1-step RT-qPCR using the GoTaq® Probe 1-Step RT-qPCR System (Cat. # A6120).
Four, tenfold dilutions of corn DNA were amplified via qPCR using the GoTaq® Probe qPCR Master Mix (Cat.# A6101) looking at the Zmm19 gene.
Four, tenfold dilutions of soybean DNA were amplified via qPCR using the GoTaq® Probe qPCR Master Mix (Cat.# A6101) looking at the PEPC17 gene.
Expression levels for the GRAS gene in oil palm seeds were evaluated via 1-step RT-qPCR using the GoTaq® 1-Step RT-qPCR System (Cat. # A6020).
Expression levels for the GAPDH gene in coffee bean were evaluated via 1-step RT-qPCR using the GoTaq® 1-Step RT-qPCR System (Cat. # A6020).
Three, tenfold dilutions of oil palm seed DNA were amplified via qPCR using the GoTaq® qPCR Master Mix (Cat.# A6001) and universal plant primers targeting the ATP-1 gene.
Three, tenfold dilutions of rose seed DNA were amplified via qPCR using the GoTaq® qPCR Master Mix (Cat.# A6001) and universal plant primers targeting the ATP-1 gene.
Three, tenfold dilutions of coffee seed DNA were amplified via qPCR using the GoTaq® qPCR Master Mix (Cat.# A6001) and universal plant primers targeting the ATP-1 gene.
DNA purified from mouse lung tissue samples was analyzed via qPCR using the GoTaq® qPCR Master Mix (Cat.# A6001) looking at three different genes (UBC, β-actin and GUSB). The GoTaq® qPCR Master Mix was able to detect all three genes when 10ng of purified DNA (ReliaPrep™ gDNA Miniprep System) was added to each reaction well.
DNA purified from mouse kidney tissue samples was analyzed via qPCR using the GoTaq® qPCR Master Mix (Cat.# A6001) looking at three different genes (UBC, β-actin and GUSB). The GoTaq® qPCR Master Mix was able to detect all three genes when 10ng of purified DNA (ReliaPrep™ gDNA Miniprep System) was added to each reaction well.
DNA purified from mouse heart tissue samples was analyzed via qPCR using the GoTaq® qPCR Master Mix (Cat.# A6001) looking at three different genes (UBC, β-actin and GUSB). The GoTaq® qPCR Master Mix was able to detect all three genes when 10ng of purified DNA (ReliaPrep™ gDNA Miniprep System) was added to each reaction well.
DNA purified from mouse lung tissue samples was analyzed via qPCR using the GoTaq® Probe qPCR Master Mix (Cat.# A6101) looking at three different genes (UBC, β-actin and GUSB). The GoTaq® Probe qPCR Master Mix was able to detect all three genes when 10ng of purified DNA (ReliaPrep™ gDNA Miniprep System) was added to each reaction well.
DNA purified from mouse kidney tissue samples was analyzed via qPCR using the GoTaq® Probe qPCR Master Mix (Cat.# A6101) looking at three different genes (UBC, β-actin and GUSB). The GoTaq® Probe qPCR Master Mix was able to detect all three genes when 10ng of purified DNA (ReliaPrep™ gDNA Miniprep System) was added to each reaction well.
DNA purified from mouse heart tissue samples was analyzed via qPCR using the GoTaq® Probe qPCR Master Mix (Cat.# A6101) looking at three different genes (UBC, β-actin and GUSB). The GoTaq® Probe qPCR Master Mix was able to detect all three genes when 10ng of purified DNA (ReliaPrep™ gDNA Miniprep System) was added to each reaction well.
Gene expression levels of B2M, GNB2L1, and HPRT1 were determined via RT-qPCR using 10ng of RNA purified from mouse lung tissue and the GoTaq® 1-Step RT-qPCR System (Cat. # A6020). The GoTaq® 1-Step RT-qPCR System was able to detect high (B2M), medium (GNB2L1), and low (HPRT1) expressed genes from mouse lung tissue.
Gene expression levels of B2M, GNB2L1, and HPRT1 were determined via RT-qPCR using 10ng of RNA purified from mouse kidney tissue and the GoTaq® 1-Step RT-qPCR System (Cat. # A6020). The GoTaq® 1-Step RT-qPCR System was able to detect high (B2M), medium (GNB2L1), and low (HPRT1) expressed genes from mouse kidney tissue.
Gene expression levels of B2M, GNB2L1, and HPRT1 were determined via RT-qPCR using 10ng of RNA purified from mouse heart tissue and the GoTaq® 1-Step RT-qPCR System (Cat. # A6020). The GoTaq® 1-Ste RT-qPCR System was able to detect high (B2M), medium (GNB2L1), and low (HPRT1) expressed genes from mouse heart tissue.
Gene expression levels of B2M, GNB2L1, and HPRT1 were determined via RT-qPCR using 10ng of RNA purified from mouse lung tissue and the GoTaq® Probe 1-Step RT-qPCR System (Cat. # A6120). The GoTaq® Probe 1-Step RT-qPCR System was able to detect all three low expressed genes from mouse lung tissue.
Gene expression levels of B2M, GNB2L1, and HPRT1 were determined via RT-qPCR using 10ng of RNA purified from mouse kidney tissue and the GoTaq® Probe 1-Step RT-qPCR System (Cat. # A6120). The GoTaq® Probe 1-Step RT-qPCR System was able to detect high (B2M), medium (GNB2L1), and low (HPRT1) expressed genes from mouse kidney tissue.
Gene expression levels of B2M, GNB2L1, and HPRT1 were determined via RT-qPCR using 10ng of RNA purified from mouse heart tissue and the GoTaq® Probe 1-Step RT-qPCR System (Cat. # A6120). The GoTaq® Probe 1-Step RT-qPCR System was able to detect high (B2M), medium (GNB2L1), and low (HPRT1) expressed genes from mouse heart tissue.
Human plasma (300µl) was spiked with inactivated CMV particles, followed by DNA extraction using the Maxwell® RSC Viral Total Nucleic Acid Purification Kit on the Maxwell® RSC instrument. CMV copies ranging from 10,000 to 100 were detected via qPCR using the GoTaq® Probe qPCR Master Mix (Cat. # A6101) on a Bio-Rad CFX96 instrument.
DNA was purified from Maize powder using the Maxwell® 16 Plant DNA Kit on a Maxwell® 16 instrument. Amplification was performed using maize Mhmg (Cy5), NOS (FAM), and P35S (JOE) assays in singleplex (Panels A-C) and triplex (Panel D) reactions using the GoTaq® Probe qPCR Master Mix (Cat. # A6101) on an ABI 7500 Real-Time PCR System.
DNA was purified from Maize powder using the Maxwell® 16 Plant DNA Kit on a Maxwell® 16 instrument. Amplification was performed using maize Mhmg (Cy5), NOS (FAM), and P35S (JOE) assays in singleplex reactions using the GoTaq® Probe qPCR Master Mix (Cat. # A6101) on an ABI 7500 Real-Time PCR System.
DNA was purified from Maize powder using the Maxwell® 16 Plant DNA Kit on a Maxwell® 16 instrument. Amplification was performed using maize Mhmg (Cy5), NOS (FAM), and P35S (JOE) assays in singleplex reactions using the GoTaq® Probe qPCR Master Mix (Cat. # A6101) on an ABI 7500 Real-Time PCR System.
DNA was purified from Maize powder using the Maxwell® 16 Plant DNA Kit on a Maxwell® 16 instrument. Amplification was performed using maize Mhmg (Cy5), NOS (FAM), and P35S (JOE) assays in triplex reactions using the GoTaq® Probe qPCR Master Mix (Cat. # A6101) on an ABI 7500 Real-Time PCR System.
Gene expression of B2M (VIC), HPRT (FAM), RNaseP (ABY), and GAPDH (JUN) was analyzed from commercially available total human colon RNA in singleplex using the GoTaq® Probe 1-Step RT-qPCR System (Cat.# A6120) on an ABI 7500 FAST Instrument.
Gene expression of RNaseP (ABY) was analyzed from commercially available total human colon RNA in singleplex using the GoTaq® Probe 1-Step RT-qPCR System (Cat.# A6120) on an ABI 7500 FAST Instrument.
Gene expression of B2M (VIC), HPRT (FAM), RNaseP (ABY), and GAPDH (JUN) was analyzed from commercially available total human colon RNA in singleplex using the GoTaq® Probe 1-Step RT-qPCR System (Cat.# A6120) on an ABI 7500 FAST Instrument.
Gene expression of B2M (VIC), HPRT (FAM), RNaseP (ABY), and GAPDH (JUN) was analyzed from commercially available total human colon RNA in quadruplex using the GoTaq® Probe 1-Step RT-qPCR System (Cat.# A6120) on an ABI 7500 FAST Instrument.
Gene expression of RNaseP (ABY), GAPDH (JUN), HPRT (FAM), and B2M (VIC) was analyzed from 20ng of RNA purified from human colon FFPE blocks in singleplex and quadruplex using the GoTaq® Probe 1-Step RT-qPCR System (Cat. # A6120) on an ABI 7500 FAST instrument.
Gene expression of RNaseP (ABY), GAPDH (JUN), HPRT (FAM), and B2M (VIC) was analyzed from 20ng of RNA purified from HCT116 cells in singleplex and quadruplex using the GoTaq® Probe 1-Step RT-qPCR System (Cat. # A6120) on an ABI 7500 FAST instrument.
Gene expression of B2M (VIC), HPRT (FAM),GAPDH (JUN), and ß-actin (Cy5) was analyzed from commercially available total human colon RNA in singleplex using the GoTaq® Probe 1-Step RT-qPCR System (Cat. # A6120) on an ABI 7500 FAST instrument.
Gene expression of B2M (VIC), HPRT (FAM),GAPDH (JUN), and ß-actin (Cy5) was analyzed from commercially available total human colon RNA in singleplex using the GoTaq® Probe 1-Step RT-qPCR System (Cat. # A6120) on an ABI 7500 FAST instrument.
Gene expression of B2M (VIC), HPRT (FAM),GAPDH (JUN), and ß-actin (Cy5) was analyzed from commercially available total human colon RNA in singleplex using the GoTaq® Probe 1-Step RT-qPCR System (Cat. # A6120) on an ABI 7500 FAST instrument.
Gene expression of B2M (VIC), HPRT (FAM),GAPDH (JUN), and ß-actin (Cy5) was analyzed from commercially available total human colon RNA in singleplex using the GoTaq® Probe 1-Step RT-qPCR System (Cat. # A6120) on an ABI 7500 FAST instrument.
Gene expression of B2M (VIC), HPRT (FAM), GAPDH (JUN) and ß-actin (Cy5) was analyzed from 20ng of RNA purified from human lung FFPE blocks in singleplex and quadruplex using the GoTaq® Probe 1-Step RT-qPCR System (Cat. # A6120) on an ABI 7500 FAST instrument.
Gene expression of B2M (VIC), HPRT (FAM), GAPDH (JUN) and ß-actin (Cy5) was analyzed from 20ng of RNA purified from HCT116 cells in singleplex and quadruplex using the GoTaq® Probe 1-Step RT-qPCR System (Cat. # A6120) on an ABI 7500 FAST instrument.
Expression of ß-actin (Cy5), CYP2D6 (FAM), and RNaseP (VIC) was analyzed from commercially available total human genomic DNA and triplex.
Expression of ß-actin (Cy5), CYP2D6 (FAM), and RNaseP (VIC) was analyzed from commercially available total human genomic DNA and triplex.
Expression of ß-actin (Cy5), CYP2D6 (FAM), and RNaseP (VIC) was analyzed from commercially available total human genomic DNA using the GoTaq® Probe qPCR Master Mix (Cat. # A6101) on an ABI 7500 FAST instrument.
Expression of ß-actin (Cy5), CYP2D6 (FAM), and RNaseP (VIC) was analyzed from 20ng of DNA purified from human lung FFPE blocks in singleplex and triplex using the GoTaq® Probe qPCR Master Mix (Cat. # A6101) on an ABI 7500 FAST instrument.
Expression of ß-actin (Cy5), CYP2D6 (FAM), and RNaseP (VIC) was analyzed from 20ng of DNA purified from human ccfDNA samples in singleplex and triplex using the GoTaq® Probe qPCR Master Mix (Cat. # A6101) on an ABI 7500 FAST instrument.
Expression of ß-actin (Cy5), CYP2D6 (FAM), and RNaseP (VIC) was analyzed from 20ng of DNA purified from human genomic DNA in singleplex and triplex using the GoTaq® Probe qPCR Master Mix (Cat. # A6101) on an ABI 7500 FAST instrument.
Gene expression of ß-actin (Cy5), HPRT (FAM), and B2M (VIC) was analyzed from 20ng of RNA purified from human lung FFPE blocks in singleplex and quadruplex using the GoTaq® Probe 1-Step RT-qPCR System (Cat. # A6120) on a Roche Lightcycler 480 instrument.
Gene expression of ß-actin (Cy5), HPRT (FAM), and B2M (VIC) was analyzed from 20ng of RNA purified from HCT116 cells in singleplex and quadruplex using the GoTaq® Probe 1-Step RT-qPCR System (Cat. # A6120) on a Roche Lightcycler 480 instrument.
Gene expression of ß-actin (Cy5), HPRT (FAM), and B2M (VIC) was analyzed from 20ng of commercially available human colon RNA in singleplex and quadruplex using the GoTaq® Probe 1-Step RT-qPCR System (Cat. # A6120) on a Roche Lightcycler 480 instrument.
Expression of ß-actin (Cy5), HPRT (FAM), and B2M (VIC) was analyzed from 20ng of DNA purified from human gDNA in singleplex and triplex using the GoTaq® Probe qPCR Master Mix (Cat. # A6101) on a Roche Lightcycler 480 instrument.
Expression of ß-actin (Cy5), HPRT (FAM), and B2M (VIC) was analyzed from 20ng of DNA purified from ccfDNA in singleplex and triplex using the GoTaq® Probe qPCR Master Mix (Cat. # A6101) on a Roche Lightcycler 480 instrument.
Expression of ß-actin (Cy5), HPRT (FAM), and B2M (VIC) was analyzed from 20ng of DNA purified from human lung FFPE blcoks in singleplex and triplex using the GoTaq® Probe qPCR Master Mix (Cat. # A6101) on a Roche Lightcycler 480 instrument.
The 16S rRNA gene found in E. coli was detected from ten-fold serial dilutions of E. coli DNA ranging from 37ng to 3.7×10–3ng using the GoTaq® qPCR Master Mix.
The 16S rRNA gene found in S. aureus was detected from ten fold serial dilutions of S. aureus DNA ranging from 126ng to 0.0126ng using the GoTaq® qPCR Master Mix.
The 16S rRNA gene found in Salmonella enterica was detected from ten fold serial dilutions of Salmonella enterica DNA ranging from 500,000fg to 50fg using the GoTaq® qPCR Master Mix.
The stx1 gene found in E. coli was detected from ten fold serial dilutions of E. coli DNA ranging from 37ng to 3.7pg using the GoTaq® Probe qPCR Master Mix.
The nucA gene found in S. aureus was detected from ten fold serial dilutions of S. aureus DNA ranging from 126ng to 0.0126ng using the GoTaq® Probe qPCR Master Mix.
The ttr gene found in Salmonella enterica was detected from ten fold serial dilutions of Salmonella enterica DNA ranging from 500pg to 0.5pg using the GoTaq® Probe qPCR Master Mix.
The hly gene found in Listeria monocytogenes was detected from ten fold serial dilutions of Listeria monocytogenes DNA ranging from 500pg to 0.5pg using the GoTaq® Probe qPCR Master Mix.
A set of predetermined Armored HIV RNA copies were evaluated via RT-qPCR using the GoTaq® Probe 1-Step RT-qPCR System (Cat.# A6120) in order to create a standard curve for HIV copy number determination in samples.
Cell culture medium was spiked with 12,500–50,000 copies of Armored HIV, followed by RNA extraction using the Maxwell® RSC Viral Total Nucleic Acid Purification Kit on the Maxwell® RSC instrument. HIV RNA was detected via qPCR using the GoTaq® Probe 1- Step RT-qPCR System (Cat. # A6120) on a Bio-Rad CFX96 instrument.

Suitable for Different Organisms and Sample Types

DNA/RNA have been isolated with GoTaq® qPCR Systems from the following organisms and sample types. DNA/RNA from organisms and sample types not listed may also be compatible—please enquire with Promega technical support for additional compatibility.

Organism Types:Sample Types:
  • Animal
  • Bacteria
  • Fungi
  • Human
  • Parasites
  • Viruses
  • Yeast












  • Blood
  • Cells
  • Feces
  • FFPE
  • Food
  • Human Cerebrospinal Fluid (CSF)
  • Plants
  • Plasma
  • Saliva
  • Serum
  • Sputum
  • Swabs
  • Tissue
  • Urine


Compatible with these Instruments

For further details on instrument compatibility, please reference the appropriate Technical Manual. Instruments not listed may also be compatible—please enquire with Promega technical support for additional compatibility.

  • Applied Biosystems ABI PRISM® 7000 and 7700 Sequence Detection System
  • Applied Biosystems 7300 and 7900HT Real-Time PCR System
  • Applied Biosystems GeneAmp® 5700 Thermal Cycler
  • Applied Biosystems StepOne™ and StepOnePlus™ Real-Time PCR Systems
  • Applied Biosystems 7500 and 7500 FAST Real-Time PCR System
  • Bio-Rad CFX96 Real-Time PCR Detection System
  • Bio-Rad DNA Engine Opticon® and Opticon® 2 Real Time PCR Detection Systems
  • Bio-Rad iCycler® iQ™ and iQ™ 5 Real-Time PCR Detection System
  • Bio-Rad/MJ Research Chromo4™ Real-Time Detector
  • Bio-Rad MyiQ™ Real-Time PCR Detection System
  • Cepheid SmartCycler® System
  • Corbett Rotor-Gene™ 3000 and 6000 Real-Time Rotary Analyzer
  • Eppendorf Mastercycler® ep realplex Real-Time PCR System
  • Roche LightCycler® 480 Real-Time PCR System
  • Stratagene Mx3000P® and Mx3005P® Real-Time PCR Systems
  • Stratagene Mx4000® Multiplex Quantitative PCR System

Specifications

You are viewing: A6001 Change Configuration

What's in the box?

Item Part # SizeAvailable Separately

GoTaq® qPCR Master Mix, 2X

A600A 5 × 1ml

CXR Reference Dye

C541A 1 × 100μl View Product

Nuclease-Free Water

P119E 2 × 13ml View Product

SDS

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Certificate of Analysis

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Use Restrictions

For Research Use Only. Not for Use in Diagnostic Procedures.

Storage Conditions

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Patents and Disclaimers

U.S. Pat. No. 6,242,235, Australian Pat. No. 761757, Canadian Pat. No. 2,335,153 and other patents and patents pending.

U.S. Pat. Nos. 8,598,198 and 9,206,474 and other patents and patents pending.

Specifications

You are viewing: A6002 Change Configuration

What's in the box?

Item Part # SizeAvailable Separately

GoTaq® qPCR Master Mix, 2X

A600A 25 × 1ml

CXR Reference Dye

C541A 5 × 100μl View Product

Nuclease-Free Water

P119E 10 × 13ml View Product

SDS

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Certificate of Analysis

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Use Restrictions

For Research Use Only. Not for Use in Diagnostic Procedures.

Storage Conditions

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Patents and Disclaimers

U.S. Pat. No. 6,242,235, Australian Pat. No. 761757, Canadian Pat. No. 2,335,153 and other patents and patents pending.

U.S. Pat. Nos. 8,598,198 and 9,206,474 and other patents and patents pending.

Specifications

You are viewing: A6020 Change Configuration

What's in the box?

Item Part # SizeConcentrationAvailable Separately

MgCl2

A351B 1 × 750μl25mM View Product

GoTaq® qPCR Master Mix, 2X

A600A 5 × 1ml

Nuclease-Free Water

P119E 2 × 13ml View Product

CXR Reference Dye

C541B 1 × 200μl30μM View Product

GoScript™ RT Mix for 1-Step RT-qPCR

M700A 1 × 225μl50X

SDS

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Certificate of Analysis

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Use Restrictions

For Research Use Only. Not for Use in Diagnostic Procedures.

Storage Conditions

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Patents and Disclaimers

U.S. Pat. No. 6,242,235, Australian Pat. No. 761757, Canadian Pat. No. 2,335,153 and other patents and patents pending.

U.S. Pat. Nos. 8,598,198 and 9,206,474 and other patents and patents pending.

Specifications

You are viewing: A6010 Change Configuration

What's in the box?

Item Part # SizeConcentrationAvailable Separately

MgCl2

A351B 1 × 750μl25mM View Product

GoScript™ 5X Reaction Buffer

A500B 1 × 300μl View Product

GoScript™ Reverse Transcriptase

A501B 1 × 50μl

GoTaq® qPCR Master Mix, 2X

A600A 5 × 1ml

Oligo(dT)15 Primer

C110B 1 × 50μg500μg/ml View Product

PCR Nucleotide Mix

C114G 1 × 200μl10mM View Product

Random Primers

C118B 1 × 50μg View Product

CXR Reference Dye

C541A 1 × 100μl View Product

Recombinant RNasin® Ribonuclease Inhibitor

N251A 1 × 2,500u40u/μl

Nuclease-Free Water

P119E 2 × 13ml View Product

SDS

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Certificate of Analysis

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Use Restrictions

For Research Use Only. Not for Use in Diagnostic Procedures.

Storage Conditions

BB

Patents and Disclaimers

U.S. Pat. No. 6,242,235, Australian Pat. No. 761757, Canadian Pat. No. 2,335,153 and other patents and patents pending.

U.S. Pat. Nos. 8,598,198 and 9,206,474 and other patents and patents pending.