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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

Code UNSPSC :
41106303
Nomenclature NACRES :
NA.55

Utilisation

sufficient for 100 reactions

Caractéristiques

dNTPs included
hotstart

Technique(s)

RT-PCR: suitable

Couleur

colorless

Entrée

purified RNA

Conditions d'expédition

wet ice

Température de stockage

−20°C

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Description générale

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.

Caractéristiques et avantages

  • 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.

Autres remarques

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.

Informations légales

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

Composants de kit également disponibles séparément

Réf. du produit
Description
FDS

  • O4387Random nonamers 100 μLFDS

  • O4387Anchored oligo(dT)23 primers 100 μLFDS

  • B017410x reaction buffers 10x AccuTaq bufferFDS

  • P219210 mM dNTP mix 10 x PCR bufferFDS

  • W1754Nuclease-free water 4 x 1.5FDS

Mentions de danger

Conseils de prudence

Classification des risques

Aquatic Chronic 3

Code de la classe de stockage

10 - Combustible liquids

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

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
Samantha Reese et al.
Journal of fungi (Basel, Switzerland), 7(7) (2021-07-03)
Fungal cell wall receptors relay messages about the state of the cell wall to the nucleus through the Cell Wall Integrity Signaling (CWIS) pathway. The ultimate role of the CWIS pathway is to coordinate repair of cell wall damage and
Anita Abu-Daya et al.
Developmental biology, 349(2), 204-212 (2010-10-28)
While limb regeneration has been extensively studied in amphibians, little is known about the initial events in limb formation in metamorphosing anurans. The small secreted integrin ligand nephronectin (npnt) is necessary for development of the metanephros in mouse. Although expressed
Samantha Reese et al.
Journal of fungi (Basel, Switzerland), 7(7) (2021-07-03)
Fungal cell wall receptors relay messages about the state of the cell wall to the nucleus through the Cell Wall Integrity Signaling (CWIS) pathway. The ultimate role of the CWIS pathway is to coordinate repair of cell wall damage and
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)

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.

Protocoles

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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