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MABE1933

Sigma-Aldrich

Anti-ASXL1 Antibody, clone 12F9

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About This Item

分類程式碼代碼:
12352203
NACRES:
NA.41

生物源

rat

品質等級

共軛

unconjugated

抗體表格

purified antibody

抗體產品種類

primary antibodies

無性繁殖

12F9, monoclonal

分子量

calculated mol wt 165.14 kDa
observed mol wt ~165 kDa

純化經由

using protein G

物種活性

human

包裝

antibody small pack of 100 μg

技術

immunocytochemistry: suitable
western blot: suitable

同型

IgG2aκ

表位序列

N-terminal

Protein ID登錄號

UniProt登錄號

運輸包裝

2-8°C

目標翻譯後修改

unmodified

基因資訊

human ... ASXL1(171023)

一般說明

Polycomb group protein ASXL1 (UniProt: Q8IXJ9; also known as Additional sex combs-like protein 1) is encoded by the ASXL1 (also known as KIAA0978) gene (Gene ID: 171023) in human. ASXL1 is a member of the ASXL family that is expressed at low levels in various tissues. However, higher expression is reported in testes. It is a member of the ASXL family with a highly conserved ASX homology (ASXH) domain at the N-terminal region and a plant homeodomain (PHD) finger (aa 1503-1540) at the C-terminal region. The ASXH domain mediates its interaction with a partner protein BAP1, which is an essential component of the polycomb repressive deubiquinase complex (PR-DUB), in which it is involved in deubiquitination of monoubiquitinated histone H2A at lysine 119 (H2AK119ub). ASXL1 also acts as a sensor of N6-methyladenosine methylation on DNA (m6A). It recognizes and binds m6A DNA, leading to its ubiquitination and degradation by TRIP12, thereby inactivating the PR-DUB complex and regulating polycomb silencing. Its HARE-HTH-type domain (aa 11-86) recognizes and binds m6A. Mutations in ASXL1 gene are known to perturb development and cause Bohring-Opitz syndrome that is characterized by severe intrauterine growth retardation, poor feeding, and mental retardation. Some mutations are also observed in myeloid neoplasms, including myelodysplastic syndromes, chronic myelomonocytic leukemia, and acute myeloid leukemia and are associated with poor prognosis. (Ref.: Matheus, F., et al. (2019). Stem Cell Reports 12(5); 861-868; Asada, S., et al. (2018). Nat. Commun. 9: Article 2733; Scheuermann, JC., et al. (2010). Nature. 465(7295); 243-247).

特異性

Clone 12F9 is a rat monoclonal antibody that detects human Polycomb group protein ASXL1.

免疫原

His-tagged recombinant fragment corresponding to the first 618 amino acids from the N-terminal region of human Polycomb group protein ASXL1.

應用

Quality Control Testing

Evaluated by Western Blotting in Human spleen tissue lysate.

Western Blotting Analysis: A 1:1,000 dilution of this antibody detected ASXL1 in Huma spleen tissue lysate.

Tested Applications

Immunocytochemistry Analysis: A representative lot detected ASXL1 in Immunocytochemistry applications (Matheus, F.. et al. (2019). Stem Cell Reports. 12(5):861-868).

Western Blotting Analysis: A representative lot detected ASXL1 in Western Blotting applications (Matheus, F.. et al. (2019). Stem Cell Reports. 12(5):861-868).

Note: Actual optimal working dilutions must be determined by end user as specimens, and experimental conditions may vary with the end user
Anti-ASXL1, clone 12F9, Cat. No. MABE1933, is a rat monoclonal antibody that detects ASXL1 and is tested for use in Immunocytochemistry and Western Blotting.

外觀

Purified rat monoclonal antibody IgG2a 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

Recommend storage at +2°C to +8°C. For long term storage antibodies can be kept at -20°C. Avoid repeated freeze-thaws.

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


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