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SAMD7 抗体

This anti-SAMD7 antibody is a 兔 多克隆 antibody detecting SAMD7 in IF (p) 和 IHC (p). Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN1387671
发货至: 中国

Quick Overview for SAMD7 抗体 (ABIN1387671)

抗原

SAMD7 (Sterile alpha Motif Domain Containing 7 (SAMD7))

适用

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人, 小鼠, 大鼠

宿主

  • 36

克隆类型

  • 36
多克隆

标记

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This SAMD7 antibody is un-conjugated

应用范围

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Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 交叉反应

    人, 小鼠, 大鼠

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human SAMD7

    亚型

    IgG
  • 应用备注

    IHC-P 1:200-400
    IF(IHC-P) 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

    This product contains ProClin: 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

    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

    有效期

    12 months
  • 抗原

    SAMD7 (Sterile alpha Motif Domain Containing 7 (SAMD7))

    别名

    SAMD7

    背景

    Synonyms: SAM domain-containing protein 7, Samd7, Samd 7, Samd-7, SAMD7_HUMAN, sterile alpha mot domain containing 7, Sterile alpha mot domain-containing protein 7.

    Background: The sterile alpha motif (SAM) domain is a 70 residue structure found in a large number of proteins involved in diverse processes present throughout the eukaryotes. The SAM domain is known to bind RNA and is arranged in a small five-helix bundle with two large interfaces. SAMD7 (Sterile alpha motif domain-containing protein 7), is a 446 amino acid protein encoded by the SAMD7 gene which maps to human chromosome 3. Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.

    基因ID

    344658
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