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形狀
lyophilized
品質等級
用途
sufficient for ≤400 reactions
包裝
pkg of 2 mg (Primer, Random pd(N)6 Potassium Salt)
製造商／商標名
Roche
儲存溫度
−20°C
一般說明
p(dN)6
應用
cDNA合成引物
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
- 将RNA样本逆转录为cDNA
- 微滴数字PCR(ddPCR)法以RNA合成cDNA
特點和優勢
- 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
其他說明
仅用于生命科学研究。不可用于诊断。
儲存類別代碼
12 - Non Combustible Liquids
水污染物質分類（WGK）
nwg
閃點（°F）
does not flash
閃點（°C）
does not flash
其他客户在看
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
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
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
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
Marie Rieux et al.
Molecular psychiatry, 26(9), 5441-5463 (2020-06-10)
Huntington's disease (HD) is a monogenic neurodegenerative disorder resulting from a mutation in the huntingtin gene. This leads to the expression of the mutant huntingtin protein (mHTT) which provokes pathological changes in both the central nervous system (CNS) and periphery.
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