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重要文件

MABE453

Sigma-Aldrich

Anti-monoubiquityl Histone H2B (Lys119) Antibody, clone 7B4

clone 7B4, from mouse

同義詞:

H2BUb1, Histone H2B type 1-C/E/F/G/I, Histone H2B.1 A, Histone H2B.a, H2B/a, Histone H2B.g, H2B/g, Histone H2B.h, H2B/h, Histone H2B.k, H2B/k, Histone H2B.l, H2B/l, H2BUbK119, H2BK119Ub

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About This Item

分類程式碼代碼:
12352203
eCl@ss:
32160702
NACRES:
NA.41

生物源

mouse

品質等級

抗體表格

purified immunoglobulin

抗體產品種類

primary antibodies

無性繁殖

7B4, monoclonal

物種活性

human

技術

immunohistochemistry: suitable
western blot: suitable

同型

IgG2aκ

NCBI登錄號

UniProt登錄號

運輸包裝

wet ice

目標翻譯後修改

unmodified

基因資訊

一般說明

H2BUb1, also known as Histone H2B.1 A, or Histone H2B.a (H2B/a), or Histone H2B.g (H2B/g), or Histone H2B.h (H2B/h), or Histone H2B.k (H2B/k) or Histone H2B.i (H2B/I;H2B/I), and encoded by the gene HIST1H2BC or HIST1H2BE, HIST1H2BF, HIST1H2BG, HIST1H2BI/H2BFL, H2BFH, H2BFG, H2BFA, H2BFK, is a core component of the nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. H2BUb1 also has broad antibacterial activity and may contribute to the formation of the functional antimicrobial barrier of the colonic epithelium, and to the bactericidal activity of amniotic fluid. H2BUb1 is localized to the nucleus and chromosomes in healthy cells.

免疫原

Ovalbumin-conjugated corresponding to human monoubiquityl Histone H2B (Lys119).

應用

Detect Histone H2B using this mouse monoclonal antibody, Anti-monoubiquityl Histone H2B (Lys119) Antibody, clone 7B4 validated for use in western blotting & IHC.
Research Category
Epigenetics & Nuclear Function
Research Sub Category
Histones
Western Blotting Analysis: A representative lot detected monoubiquityl Histone H2B (Lys119) in hormone deprived MCF7 cell lysates, which were pretreated with vehicle (ethanol) or Bortezomid before incubating with 17Beta-Estradiol (Prenzel, T., et al. (2011). AACR. OF1-OF15).
Western Blotting Analysis: A representative lot detected monoubiquityl Histone H2B (Lys119) in differentiated hMSCs that were truncated with control and demostrated a loss of signal in differntiated hMSCs that ere transfected with RNF50 siRNA (Karpiuk, O., et al. (2012). Molecular Cell. 46:705-713).
Immunohistochemistry Analysis: A representative lot detected monoubiquityl Histone H2B (Lys119) in malignant, metastatic breast tumor and normal adjacent tissues (Prenzel, T., et al. (2011). AACR. OF1-OF15).

品質

Evaluated by Western Blotting in HeLa cell lysate.

Western Blotting Analysis: 0.5 µg/mL of this antibody detected monoubiquityl Histone H2B (Lys119) in HeLa cell lysates treated with and without Nocodazole.

標靶描述

~20 kDa observed

外觀

Protein G Purified
Format: Purified
Purified mouse monoclonal IgG2aκ in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

儲存和穩定性

Stable for 1 year at 2-8°C from date of receipt.

其他說明

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

免責聲明

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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儲存類別代碼

12 - Non Combustible Liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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The histone H2B monoubiquitination regulatory pathway is required for differentiation of multipotent stem cells.
Karpiuk, Oleksandra, et al.
Molecular Cell, 46, 705-713 (2012)
Mei-Jun Zhao et al.
Oncotarget, 7(8), 8956-8967 (2016-01-21)
The ubiquitin ligase RNF8 promotes the DNA damage response (DDR). We observed that the expression of RNF8 was increased in bladder cancer cells and that this change in RNF8 expression could be reversed by adenovirus-mediated shRNA treatment. Moreover, we found

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