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BSDC1 抗体 (C-Term)

This anti-BSDC1 antibody is a 兔 多克隆 antibody detecting BSDC1 in WB 和 EIA. Suitable for 人.
产品编号 ABIN950682
发货至: 中国

Quick Overview for BSDC1 抗体 (C-Term) (ABIN950682)

抗原

See all BSDC1 抗体
BSDC1 (BSD Domain Containing 1 (BSDC1))

适用

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宿主

  • 16

克隆类型

  • 16
多克隆

标记

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This BSDC1 antibody is un-conjugated

应用范围

  • 16
  • 8
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Western Blotting (WB), Enzyme Immunoassay (EIA)
  • 抗原表位

    • 8
    • 3
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    • 1
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    • 1
    AA 396-425, C-Term

    特异性

    This antibody reacts to BSDC1.

    交叉反应 (详细)

    Species reactivity (tested):Human.

    纯化方法

    Affinity chromatography on Protein A

    免疫原

    KLH conjugated synthetic peptide between 396-425 amino acids from the C-terminal region of human BSDC1

    亚型

    Ig Fraction
  • 应用备注

    Optimal working dilution should be determined by the investigator.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.25 mg/mL

    缓冲液

    PBS containing 0.09 % (W/V) sodium azide as preservative

    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.

    注意事项

    Avoid repeated freezing and thawing.

    储存条件

    4 °C/-20 °C

    储存方法

    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • 抗原

    BSDC1 (BSD Domain Containing 1 (BSDC1))

    别名

    BSDC1

    背景

    BSDC1 is a 430 amino acid protein encoded by a gene mapping to chromosome 1. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.Synonyms: BSD domain-containing protein 1

    基因ID

    55108

    NCBI登录号

    NP_060515
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