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CCDC19 抗体

CCDC19 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7190228
发货至: 中国
  • 抗原 See all CCDC19 抗体
    CCDC19 (Coiled-Coil Domain Containing 19 (CCDC19))
    适用
    • 40
    • 14
    • 12
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    宿主
    • 40
    克隆类型
    • 40
    多克隆
    标记
    • 10
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This CCDC19 antibody is un-conjugated
    应用范围
    • 34
    • 15
    • 13
    • 3
    • 1
    ELISA, Immunohistochemistry (IHC)
    交叉反应
    纯化方法
    Antigen affinity purification
    免疫原
    Synthetic peptide of Human CFAP45
    亚型
    IgG
  • 应用备注
    ELISA:1:2000-1:5000, IHC:1:25-1:100,
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol
    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
    -20 °C,-80 °C
    储存方法
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 抗原
    CCDC19 (Coiled-Coil Domain Containing 19 (CCDC19))
    别名
    CFAP45 (CCDC19 产品)
    别名
    nesg1 antibody, MGC76242 antibody, CCDC19 antibody, NESG1 antibody, 1700028D05Rik antibody, Nesg1 antibody, cilia and flagella associated protein 45 antibody, cilia and flagella associated protein 45 S homeolog antibody, coiled-coil domain-containing protein 19, mitochondrial antibody, cfap45 antibody, CFAP45 antibody, cfap45.S antibody, LOC748703 antibody, Cfap45 antibody
    背景

    Background: CCDC19 is a 466 amino acid protein encoded by a gene mapping to human 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, Parkinson's, Gaucher disease and Usher syndrome are also associated with chromosome 1.

    Aliases: CCD19_HUMAN antibody, CCDC19 antibody, Coiled coil domain containing 19 antibody, Coiled-coil domain-containing protein 19 antibody, mitochondrial antibody, Nasopharyngeal epithelium specific protein 1 antibody, Nasopharyngeal epithelium-specific protein 1 antibody, NESG1 antibody, OTTHUMP00000033461 antibody, RP11 190A12.6 antibody

    UniProt
    Q9UL16
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