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Merck
CN

U4758

Sigma-Aldrich

Anti-U2AF65 antibody, Mouse monoclonal

clone MC3, purified from hybridoma cell culture

别名:

Anti-U2AF65

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About This Item

MDL编号:
UNSPSC代码:
12352203
NACRES:
NA.41

生物来源

mouse

质量水平

偶联物

unconjugated

抗体形式

purified immunoglobulin

抗体产品类型

primary antibodies

克隆

MC3, monoclonal

表单

buffered aqueous solution

分子量

antigen ~65 kDa

种属反应性

human, rat, Xenopus, mouse

包装

antibody small pack of 25 μL

技术

electron microscopy: suitable
immunocytochemistry: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
indirect ELISA: suitable
microarray: suitable
western blot: 0.1-0.2 μg/mL using total cell extract from HeLa cells

同位素/亚型

IgG2b

UniProt登记号

运输

dry ice

储存温度

−20°C

靶向翻译后修饰

unmodified

基因信息

human ... U2AF2(11338)
mouse ... U2af2(22185)
rat ... U2af2(308335)

一般描述

Monoclonal Anti-U2AF65 (mouse IgG2b isotype) is derived from the MC3 hybridoma produced by the fusion of mouse myeloma cells (Ag8.653 cells) and splenocytes from BALB/c mice immunized with recombinant human U2AF65. U1, U2, U4/U6, and U5 are small nuclear riboprotein (snRNPs) that are major subunits of spliceosomes. Spliceosomes also contain non snRNPs proteins such as alternative splicing factor/splicing factor 2 (ASF/SF2), 35 kDa spliceosomal component (SC-35) and U2 snRNP auxiliary splicing factor (U2AF). U2 snRNP auxiliary factor 65 kDa (U2AF65) is a splicing factor which has three C-terminal RNA recognition motifs (RRMs) and an N-terminal arginine/serine-rich (RS) domain. This gene is mapped to human chromosome 19q13.42. Splicing factor U2AF65kDa subunit is a non-snRNP protein component of spliceosome complexes.

免疫原

recombinant human U2AF65.

应用

Monoclonal Anti-U2AF65 antibody produced in mouse has been used in:
  • RNA immunoprecipitation
  • immunoblotting
  • chromatin immunoprecipitation (ChIP)
  • enzyme-linked immunosorbent assay (ELISA)
  • immunohistochemistry
  • immunocytochemistry
  • immunoelectron microscopy

生化/生理作用

U2 snRNP auxiliary factor 65 kDa (U2AF65)/U2AF2 helps to supply the small nuclear ribonucleoprotein (snRNP) U2, which is subunit of the spliceosome. It can induce the exclusion of alternative exons. U2AF65 primarily regulates the splicing of pre-mRNA. The serine-rich (RS) repeats at the N-terminal region act as a signalling factor for nuclear localization. (U2AF65) and (U2AF35) are components of the splicing factor U2AF that transports between the cytoplasm and the nucleus.

外形

Solution in 0.01 M phosphate buffered saline, pH 7.4, and 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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储存分类代码

10 - Combustible liquids

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

常规特殊物品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Gloria Barbarani et al.
Scientific reports, 7(1), 14088-14088 (2017-10-28)
The Sox6 transcription factor is crucial for terminal maturation of definitive red blood cells. Sox6-null mouse fetuses present misshapen and nucleated erythrocytes, due to impaired actin assembly and cytoskeleton stability. These defects are accompanied with a reduced survival of Sox6
Splicing of many human genes involves sites embedded within introns
Kelly S, et al.
Nucleic Acids Research, 43(9), 4721-4732 (2015)
Identification of U2AF (35)-dependent exons by RNA-Seq reveals a link between 3? splice-site organization and activity of U2AF-related proteins
Kralovicova J, et al.
Nucleic Acids Research, 43(7), 3747-3763 (2015)
Splicing inhibition of U2AF65 leads to alternative exon skipping
Cho S, et al.
Proceedings of the National Academy of Sciences of the USA, 112(32), 9926-9931 (2015)
In vitro iCLIP-based modeling uncovers how the splicing factor U2AF2 relies on regulation by cofactors
Sutandy FXR, et al.
Genome Research, 28(5), 699-713 (2018)

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