C2872
Anti-CSTF1 (N-terminal) antibody produced in rabbit
~1.0 mg/mL, affinity isolated antibody, buffered aqueous solution
别名:
Anti-Cleavage stimulation factor, 3-prime PRE-RNA, subunit 1, 50-KD, Anti-CstF-50, Anti-CstFp50
生物来源
rabbit
偶联物
unconjugated
抗体形式
affinity isolated antibody
抗体产品类型
primary antibodies
克隆
polyclonal
表单
buffered aqueous solution
分子量
antigen ~48 kDa
种属反应性
human
浓度
~1.0 mg/mL
技术
immunoprecipitation (IP): 5-10 μg using K562 cell lysates
western blot: 1-2 μg/mL using HepG2 cell lysates
UniProt登记号
运输
dry ice
储存温度
−20°C
基因信息
human ... CSTF1(1477)
mouse ... Cstf1(67337)
rat ... Cstf1(311670)
一般描述
Cleavage stimulation factor (CSTF) is a heterotrimer consisting of subunits of 50, 64 and 77 kDa referred to as CSTF1, CSTF2 and CSTF3 respectively. Anti-CSTF1 (N-terminal) is produced in rabbit using a synthetic peptide as immunogen. It corresponds to amino acids 2-16 of human CSTF1 conjugated to KLH. The corresponding sequence is identical in mouse and rat. The antibody is affinity-purified using the immunizing peptide immobilized on agarose.
应用
Anti-CSTF1 is used in immunoprecipitation at a concentration of 5-10 μg using K562 cell lysates. The antibody may be used in several immunochemical techniques including immunoblotting (∼48 kDa).
生化/生理作用
CSTF1 is required for in vitro cleavage activity. CSTF1 also interacts directly with the RNA polymerase II CTD, suggesting a role in linking transcription and mRNA 3′-ends processing. It is required for polyadenylation and 3′-end cleavage of mammalian pre-mRNAs.
外形
Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.
免责声明
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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J Zhao et al.
Microbiology and molecular biology reviews : MMBR, 63(2), 405-445 (1999-06-05)
Formation of mRNA 3' ends in eukaryotes requires the interaction of transacting factors with cis-acting signal elements on the RNA precursor by two distinct mechanisms, one for the cleavage of most replication-dependent histone transcripts and the other for cleavage and
C R Mandel et al.
Cellular and molecular life sciences : CMLS, 65(7-8), 1099-1122 (2007-12-26)
Most eukaryotic mRNA precursors (premRNAs) must undergo extensive processing, including cleavage and polyadenylation at the 3'-end. Processing at the 3'-end is controlled by sequence elements in the pre-mRNA (cis elements) as well as protein factors. Despite the seeming biochemical simplicity
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