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BSDC1 抗体 (C-Term)

BSDC1 适用: 人 WB, EIA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN950682
发货至: 中国
  • 抗原 See all BSDC1 抗体
    BSDC1 (BSD Domain Containing 1 (BSDC1))
    抗原表位
    • 8
    • 8
    • 6
    • 1
    • 1
    • 1
    • 1
    AA 396-425, C-Term
    适用
    • 21
    • 5
    • 4
    • 4
    • 4
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    宿主
    • 21
    克隆类型
    • 21
    多克隆
    标记
    • 11
    • 2
    • 2
    • 2
    • 2
    • 2
    This BSDC1 antibody is un-conjugated
    应用范围
    • 21
    • 13
    • 3
    • 2
    • 1
    Western Blotting (WB), Enzyme Immunoassay (EIA)
    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
    Top Product
    Discover our top product BSDC1 Primary Antibody
  • 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 (BSDC1 产品)
    别名
    BSDC1 antibody, fb51h12 antibody, wu:fb51h12 antibody, zgc:100785 antibody, bsdc1 antibody, 1110063F24Rik antibody, AW011758 antibody, RGD1311622 antibody, BSD domain containing 1 antibody, BSD domain containing 1 L homeolog antibody, BSDC1 antibody, bsdc1 antibody, bsdc1.L antibody, Bsdc1 antibody
    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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