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HSRT100

Sigma-Aldrich

Enhanced Avian HS RT-PCR Kit

Flexible kit for one-step or two-step RT-PCR

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About This Item

UNSPSC Code:
41106303
NACRES:
NA.55

Quality Level

usage

sufficient for 100 reactions

feature

dNTPs included
hotstart

technique(s)

RT-PCR: suitable

color

colorless

input

purified RNA

shipped in

wet ice

storage temp.

−20°C

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General description

Procedures are provided for one-step and two-step RT-PCR reactions.

One-step: In a single tube, eAMV RT and AccuTaq LA act sequentially to first produce cDNA and then immediately amplify by PCR. This provides quick, sensitive analysis of RNA.

Two-step: Each reaction is individually optimized for greater yields with high fidelity, when protocol requires multiple amplifications, or if maximum yield is more important than maximum convenience.

Application

Enhanced Avian HS RT-PCR Kit has been used to synthesize the cDNA first-strand during reverse transcriptase PCR (RT-PCR) analysis.

Features and Benefits

  • Greater transcription lengths than other reverse transcriptases, generating cDNA up to 14.1 Kb.
  • Higher sensitivity for detecting low abundance messages. eAMV RT is able to transcribe RNA that other reverse transcriptases cannot detect.
  • Unsurpassed transcription through difficult secondary structure.
  • Increased sensitivity, specificity and yield from JumpStart AccuTaq LA DNA Polymerase.

Other Notes

Reverse Transcriptase PCR (RT-PCR) is a powerful tool used to study gene expression. The Enhanced Avian HS RT-PCR kit utilizes an enhanced avian myeloblastosis virus reverse transcriptase (eAMV-RT) enzyme that offers superior performance in comparison to standard AMV-RT and Moloney murine leukemia virus reverse transcriptase (MMLV-RT). eAMV RT is an exceptionally robust enzyme with an enhanced ability to transcribe through difficult secondary structure at elevated temperatures (up to 65 °C) making it the ideal enzyme for producing high quality full-length cDNA (up to 14.1 kb) from total RNA or poly(A)+ RNA. JumpStart AccuTaq LA DNA polymerase mix is also provided to eliminate non-specific amplification and increase specificity and sensitivity. The combination of these two enzymes provides a quality system that offers the versatility of a one-step or two-step RT-PCR protocol.

Legal Information

No license is conveyed with the purchase of this product under any of US Patents Nos. 5,804,375, 5,994,056, 6,171,785, 6,214,979, 5,538,848, 5,723,591, 5,876,930, 6,030,787, and 6,258,569, and corresponding patents outside the United States, or any other patents or patent applications, relating to the 5′ Nuclease and dsDNA-Binding Dye Processes. For further information contact the Director of Licensing, Applied Biosystems, 850 Lincoln Centre Drive, Foster City, California 94404, USA.
AccuTaq is a trademark of Sigma-Aldrich Co. LLC
JumpStart is a trademark of Sigma-Aldrich Co. LLC
eAMV is a trademark of Sigma-Aldrich Co. LLC

Kit Components Also Available Separately

Product No.
Description
SDS

  • O4387Random nonamers 100 μLSDS

  • O4387Anchored oligo(dT)23 primers 100 μLSDS

  • B017410x reaction buffers 10x AccuTaq bufferSDS

  • P219210 mM dNTP mix 10 x PCR bufferSDS

  • W1754Nuclease-free water 4 x 1.5SDS

Hazard Statements

Precautionary Statements

Hazard Classifications

Aquatic Chronic 3

Storage Class Code

10 - Combustible liquids

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Chelsea T Smartt et al.
The American journal of tropical medicine and hygiene, 81(2), 258-263 (2009-07-29)
Alterations in gene expression in the midgut of female Culex pipiens quinquefasciatus exposed to blood meals containing 6.8 logs plaque-forming units/mL of West Nile virus (WNV) were studied by fluorescent differential display. Twenty-six different cDNAs exhibited reproducible differences after feeding
Transgenic chickpea expressing a recombinant human $\alpha$ 1-proteinase inhibitor ($\alpha$ 1-PI) driven by a seed-specific promoters from the common bean Phaseolus vulgaris (L.)
Mishra S, et al.
Plant Cell, Tissue and Organ Culture, 115(1), 23-33 (2013)
Nicotiana tabacum osmotic stress-activated kinase is regulated by phosphorylation on Ser-154 and Ser-158 in the kinase activation loop
Burza AM, et al.
The Journal of Biological Chemistry, 281(45), 34299-34311 (2006)
17-estradiol attenuates LPS-induced interleukin-8 production by human peripheral blood monocytes through estrogen receptor-activation
Malisorn N, et al.
African Journal of Pharmacy and Pharmacology, 4(11), 806-810 (2010)
Convergent sets of data from in vivo and in vitro methods point to an active role of Hsp60 in chronic obstructive pulmonary disease pathogenesis.
Cappello F, et al.
PLoS ONE, 6, e28200-e28200 (2011)

Articles

Challenges in gene expression analysis include mRNA stability, temporal transcription patterns, and mRNA-protein correlation, impacting accuracy.

Challenges in gene expression analysis include mRNA stability, temporal transcription patterns, and mRNA-protein correlation, impacting accuracy.

Challenges in gene expression analysis include mRNA stability, temporal transcription patterns, and mRNA-protein correlation, impacting accuracy.

Challenges in gene expression analysis include mRNA stability, temporal transcription patterns, and mRNA-protein correlation, impacting accuracy.

Protocols

The 3’/5’ integrity assay identifies RNA degradation, crucial for large sample sets or less detectable degradation.

The 3’/5’ integrity assay identifies RNA degradation, crucial for large sample sets or less detectable degradation.

The 3’/5’ integrity assay identifies RNA degradation, crucial for large sample sets or less detectable degradation.

The 3’/5’ integrity assay identifies RNA degradation, crucial for large sample sets or less detectable degradation.

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