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WHSC2 抗体 (AA 280-511)

This anti-WHSC2 antibody is a 小鼠 单克隆 antibody detecting WHSC2 in WB, ELISA, IHC, FACS 和 ICC. Suitable for 人. This Primary Antibody has been cited in 2+ publications.
产品编号 ABIN1724801
发货至: 中国

Quick Overview for WHSC2 抗体 (AA 280-511) (ABIN1724801)

抗原

See all WHSC2 抗体
WHSC2 (Wolf-Hirschhorn Syndrome Candidate 2 (WHSC2))

适用

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宿主

  • 29
  • 13
  • 1
小鼠

克隆类型

  • 33
  • 10
单克隆

标记

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This WHSC2 antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Flow Cytometry (FACS), Immunocytochemistry (ICC)

克隆位点

6B11H8
  • 抗原表位

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    AA 280-511

    原理

    WHSC2 Antibody

    纯化方法

    Ascitic fluid

    免疫原

    Purified recombinant fragment of human WHSC2 (AA: 280-511) expressed in E. Coli.

    亚型

    IgG2b
  • 应用备注

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    ICC: 1/200 - 1/1000

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Ascitic fluid containing 0.03 % sodium azide.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    4 °C,-20 °C

    储存方法

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Kerzendorfer, Hannes, Colnaghi, Abramowicz, Carpenter, Vermeesch, ODriscoll: "Characterizing the functional consequences of haploinsufficiency of NELF-A (WHSC2) and SLBP identifies novel cellular phenotypes in Wolf-Hirschhorn syndrome." in: Human molecular genetics, Vol. 21, Issue 10, pp. 2181-93, (2012) (PubMed).

    Yung, Narita, Komori, Yamaguchi, Handa: "Cellular dynamics of the negative transcription elongation factor NELF." in: Experimental cell research, Vol. 315, Issue 10, pp. 1693-705, (2009) (PubMed).

  • 抗原

    WHSC2 (Wolf-Hirschhorn Syndrome Candidate 2 (WHSC2))

    别名

    WHSC2

    背景

    This gene is expressed ubiquitously with higher levels in fetal than in adult tissues. It encodes a protein sharing 93 % sequence identity with the mouse protein. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene is mapped to the 165 kb WHS critical region, and may play a role in the phenotype of the WHS or Pitt-Rogers-Danks syndrome. The encoded protein is found to be capable of reacting with HLA-A2-restricted and tumor-specific cytotoxic T lymphocytes, suggesting a target for use in specific immunotherapy for a large number of cancer patients. This protein has also been shown to be a member of the NELF (negative elongation factor) protein complex that participates in the regulation of RNA polymerase II transcription elongation.

    分子量

    57.3 kDa

    基因ID

    7469

    途径

    Chromatin Binding
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