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11034731001

Roche

引物“随机”

lyophilized, sufficient for ≤400 reactions, pkg of 2 mg (Primer, Random pd(N)6 Potassium Salt)

别名:

引物

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2 MG
$438.00

$438.00

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2 MG
$438.00

About This Item

UNSPSC代码:
41106300

$438.00

请联系客服了解存货情况

表单

lyophilized

质量水平

100

用途

sufficient for ≤400 reactions

包装

pkg of 2 mg (Primer, Random pd(N)6 Potassium Salt)

制造商/商品名称

Roche

储存温度

−20°C

相关类别

一般描述

p(dN)6

应用

cDNA合成引物[1][2][3]
随机引物已用于：
  • 逆转录聚合酶链式反应(RT-PCR)和定量PCR(qPCR)逆转录RNA[4][5]
  • 将RNA样本逆转录为cDNA[6]
  • 微滴数字PCR(ddPCR)法以RNA合成cDNA[7]

特点和优势

  • 对mRNA中的所有RNA序列具有一致的代表性
  • 可用于引发无poly(A)尾RNA的cDNA转录
  • 短cDNA转录本可克服RNA二级结构带来的难题
  • 可控制cDNA的平均长度，只要调节逆转录(RT)反应中随机引物与RNA的比例

其他说明

仅用于生命科学研究。不可用于诊断。

储存分类代码

12 - Non Combustible Liquids

WGK

nwg

闪点(°F)

does not flash

闪点(°C)

does not flash

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
48285120
40160920
32062220
23159821
66994120

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Amaresh C Panda et al.
Nucleic acids research, 44(5), 2393-2408 (2016-01-29)
Skeletal muscle contains long multinucleated and contractile structures known as muscle fibers, which arise from the fusion of myoblasts into multinucleated myotubes during myogenesis. The myogenic regulatory factor (MRF) MYF5 is the earliest to be expressed during myogenesis and functions
Vadim Alexandrov et al.
Nature biotechnology, 34(8), 838-844 (2016-07-05)
Rapid technological advances for the frequent monitoring of health parameters have raised the intriguing possibility that an individual's genotype could be predicted from phenotypic data alone. Here we used a machine learning approach to analyze the phenotypic effects of polymorphic
Monika Hiller et al.
PloS one, 13(10), e0204485-e0204485 (2018-10-03)
Duchenne muscular dystrophy is a lethal disease caused by lack of dystrophin. Skipping of exons adjacent to out-of-frame deletions has proven to restore dystrophin expression in Duchenne patients. Exon 51 has been the most studied target in both preclinical and
Vittoria Pagliarini et al.
Journal of neurochemistry, 153(2), 264-275 (2019-12-08)
Spinal muscular atrophy (SMA) is a motor neuron disease caused by loss of function mutations in the Survival Motor Neuron 1 (SMN1) gene and reduced expression of the SMN protein, leading to spinal motor neuron death, muscle weakness and atrophy.
Tae-Dong Kim et al.
The Journal of clinical investigation, 126(2), 706-720 (2016-01-06)
Histone demethylase upregulation has been observed in human cancers, yet it is unknown whether this is a bystander event or a driver of tumorigenesis. We found that overexpression of lysine-specific demethylase 4A (KDM4A, also known as JMJD2A) was positively correlated
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