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Key Documents

WH0005725M1

Sigma-Aldrich

抗 PTBP1 单克隆抗体 小鼠抗

clone 3H8, purified immunoglobulin, buffered aqueous solution

同義詞:

抗-HNRNPI, 抗-HNRPI, 抗-MGC10830, 抗-MGC8461, 抗-PTB, 抗-PTB1, 抗-PTB2, 抗-PTB3, 抗-PTB4, 抗-PTBT, 抗-pPTB, 抗-多嘧啶束结合蛋白1

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About This Item

MDL號碼:
分類程式碼代碼:
12352203
NACRES:
NA.41

生物源

mouse

共軛

unconjugated

抗體表格

purified immunoglobulin

抗體產品種類

primary antibodies

無性繁殖

3H8, monoclonal

形狀

buffered aqueous solution

物種活性

human

技術

immunohistochemistry (formalin-fixed, paraffin-embedded sections): suitable
immunoprecipitation (IP): suitable
indirect ELISA: suitable
indirect immunofluorescence: suitable
western blot: 1-5 μg/mL

同型

IgG1κ

GenBank登錄號

UniProt登錄號

運輸包裝

dry ice

儲存溫度

−20°C

目標翻譯後修改

unmodified

基因資訊

human ... PTBP1(5725)

一般說明

该基因属于普遍表达的异质核糖核蛋白(hnRNPs)的亚家族。hnRNP是RNA结合蛋白,其与异质核RNA(hnRNA)形成复合物。这些蛋白质与细胞核中的前mRNA相关,并且似乎影响前mRNA的加工以及mRNA代谢和转运的其他方面。尽管所有hnRNP存在于细胞核中,但有些似乎在细胞核和细胞质之间穿梭。hnRNP蛋白具有独特的核酸结合特性。该基因编码的蛋白质具有结合RNA的准RNA识别基序(RRM)域的四个重复序列。该蛋白质与需要前mRNA剪接的内含子聚嘧啶束结合,并通过蛋白质降解泛素-蛋白酶体途径起作用。它也可能促进U2 snRNP与前mRNA的结合。该蛋白位于核质中,也可以在核仁周围结构中检测到。已经描述了编码不同亚型的选择性剪接的转录变体。(由RefSeq提供)

免疫原

PTBP1(NP_002810, 45 a.a.~ 144 a.a)带有GST标签的部分重组蛋白。仅GST标签的MW为26 KDa。

序列
KKFKGDSRSAGVPSRVIHIRKLPIDVTEGEVISLGLPFGKVTNLLMLKGKNQAFIEMNTEEAANTMVNYYTSVTPVLRGQPIYIQFSNHKELKTDSSPNQ

外觀

溶于pH7.4的磷酸盐缓冲盐水中的溶液

法律資訊

GenBank is a registered trademark of United States Department of Health and Human Services

免責聲明

除非我们的产品目录或产品附带的其他公司文档另有说明,否则我们的产品仅供研究使用,不得用于任何其他目的,包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的消费或应用于人类或动物。

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儲存類別代碼

10 - Combustible liquids

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


分析證明 (COA)

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存取文件庫

Alfredo Castello et al.
Nature protocols, 8(3), 491-500 (2013-02-16)
Owing to their preeminent biological functions, the repertoire of expressed RNA-binding proteins (RBPs) and their activity states are highly informative about cellular systems. We have developed a novel and unbiased technique, called interactome capture, for identifying the active RBPs of
Joel I Perez-Perri et al.
Nature protocols, 16(1), 27-60 (2020-11-20)
Interactions between RNA-binding proteins (RBPs) and RNAs are critical to cell biology. However, methods to comprehensively and quantitatively assess these interactions within cells were lacking. RNA interactome capture (RIC) uses in vivo UV crosslinking, oligo(dT) capture, and proteomics to identify
Raul Guantes et al.
Genome research, 25(5), 633-644 (2015-03-25)
Noise in gene expression is a main determinant of phenotypic variability. Increasing experimental evidence suggests that genome-wide cellular constraints largely contribute to the heterogeneity observed in gene products. It is still unclear, however, which global factors affect gene expression noise
Kristine Y Tan et al.
The Analyst, 145(10), 3732-3741 (2020-04-30)
In an open microfluidic device, we investigate protein polyacrylamide gel electrophoresis (PAGE) separation performance on single-cell lysate. Single-cell protein electrophoresis is performed in a thin layer of polyacrylamide (PA) gel into which microwells are molded. Individual cells are isolated in
Manuel Garcia-Moreno et al.
Molecular cell, 74(1), 196-211 (2019-02-26)
The compendium of RNA-binding proteins (RBPs) has been greatly expanded by the development of RNA-interactome capture (RIC). However, it remained unknown if the complement of RBPs changes in response to environmental perturbations and whether these rearrangements are important. To answer these

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