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Sigma-Aldrich

增强型禽类第一链合成试剂盒

Components for cDNA synthesis with enhanced AMV reverse transcriptase

别名:

eAMV-RT, 逆转录酶 cDNA 合成试剂盒

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About This Item

分類程式碼代碼:
12352200
NACRES:
NA.55

品質等級

用途

sufficient for 50 reactions
 kit sufficient for 50 reactions

特點

dNTPs included
hotstart: no

技術

RT-PCR: suitable

顏色

colorless

輸入

purified RNA

運輸包裝

dry ice

儲存溫度

−20°C

一般說明

Sigma的cDNA第一链合成试剂盒(增强型禽类AMV-RT)还提供随机九核苷酸(9-mers)引物和anchored oligo(dT)23引物,以防有时基因特异性引物无法起效。anchored oligo由23个胸苷(T)残基和一个G、C或A残基(anchor/锚点)组成。锚点用于保证oligo(dT)引物结合在信使mRNA最起头处,不会留出一长段的未用序列。该试剂盒可产出适合各种下游应用的可靠cDNA,包括PCR。
cDNA第一链合成试剂盒(增强型鸟类AMV-RT)采用高度纯化的鸟类成髓细胞性白细胞病毒逆转录酶(eAMV-RT),与标准AMV-RT或标准莫洛尼鼠类白血病病毒逆转录酶(MMLV-RT)相比,性能更加优越。 这种更加强大的eAMV逆转录酶可在高温(高达65℃)下转录棘手的二级结构,从总RNA或poly(A)+ RNA生成高质量的全长cDNA。

應用

cDNA第一链合成试剂盒(增强型禽类AMV-RT)可用于cDNA合成,以便用于实时逆转录-聚合酶链式反应(RT-PCR)。

單位定義

一单位酶可以多聚腺苷酸为模板,以12-18长度的oligo(dT)为引物,在10分钟内将1纳摩TMP整合进TCA-沉淀材料中。

法律資訊

Purchase of this product is accompanied by a limited license for use in the Polymerase Chain Reaction (PCR) process for research purposes only and in conjunction with a thermal cycler whose use in the automated performance of the PCR process is covered by an up-front license fee, either by payment to Applied Biosystems or as purchased, i.e., and authorized thermal cycler.

仅试剂盒组分

产品编号
说明

  • Enhanced Avian Reverse Transcriptase 1000 U

试剂盒组分也可单独购买

产品编号
说明
化学品安全说明书

  • Deoxynucleotide mix 50 μL

  • O4387Anchored oligo (dT)23 100 μL化学品安全说明书

  • R7647Random nonamers 100 μL化学品安全说明书

  • O4387Ribonuclease inhibitor 50 μL化学品安全说明书

  • W1754PCR grade water 1.5 mL化学品安全说明书

儲存類別代碼

10 - Combustible liquids

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Aerosol-administered α-tocopherol attenuates lung inflammation in rats given lipopolysaccharide intratracheally.
Experimental Lung Research, 31, 34510-34524 (2007)
María José Martín et al.
The Journal of biological chemistry, 282(47), 34510-34524 (2007-09-21)
Heme oxygenase-1 (HO-1), an inducible enzyme that metabolizes the heme group, is highly expressed in human Kaposi sarcoma lesions. Its expression is up-regulated by the G protein-coupled receptor from the Kaposi sarcoma-associated herpes virus (vGPCR). Although recent evidence shows that
Heat shock proteins expression during thermal risk exposure in the temperate xerothermic ant Formica cinerea
Slipinski P, et al.
Sociobiology, 62(3), 457-459 (2015)
Sigma-Aldrich Corporation's Life Science Quarterly. Hot Start RT-PCR results in improved performance of the enhanced Avian RT-PCR
Easlund, E., and Mueller, E.
Sigma data, 2-5 (2001)
E M Brooks et al.
BioTechniques, 19(5), 806-812 (1995-11-01)
The secondary structure in mRNA is essential for many processes, but it can present a technical problem in making full-length cDNA with reverse transcriptases. Furthermore, different reverse transcriptases have differing abilities to transcribe through regions with secondary structure, which can

商品

One approach to the analysis of gene expression is to measure the concentration of mRNA of a gene. There are several challenges to such analyses, such as the differences in half life between different transcripts, the temporal patterns of transcription and the lack of correlation between mRNA and protein.

实验方案

The 3’/5’ integrity assay is a potential first step in the identification of RNA degradation. The assay is particularly useful when a large number of samples are to be analyzed or when the degradation is less than that detected by capillary systems but still sufficient to effect qPCR analyses.

相关内容

Quantitative PCR (qPCR) or quantitative Real-Time PCR applications, utilizing fluorescent report molecules, suitable for your microRNA, genotyping, and gene expression analyses.

Polymerase chain reaction (PCR) is a technique for amplifying nucleic acid molecules and is commonly used in many applications, including RT-PCR, hot start PCR, end point PCR and more.

Polymerase chain reaction (PCR) is a technique for amplifying nucleic acid molecules and is commonly used in many applications, including RT-PCR, hot start PCR, end point PCR and more.

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