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PDZD9 抗体 (AA 50-100)

PDZD9 适用: 人, 大鼠, 小鼠 WB, IF (p), IHC (p) 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN1387114
发货至: 中国
  • 抗原 See all PDZD9 抗体
    PDZD9 (PDZ Domain Containing 9 (PDZD9))
    抗原表位
    • 14
    • 1
    • 1
    AA 50-100
    适用
    • 17
    • 15
    • 14
    • 2
    • 1
    人, 大鼠, 小鼠
    宿主
    • 16
    • 1
    克隆类型
    • 17
    多克隆
    标记
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This PDZD9 antibody is un-conjugated
    应用范围
    Western Blotting (WB), 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 PDZD9
    亚型
    IgG
  • 应用备注
    WB 1:300-5000
    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
    PDZD9 (PDZ Domain Containing 9 (PDZD9))
    别名
    PDZD9 (PDZD9 产品)
    别名
    C16orf65 antibody, C25H16orf65 antibody, 4930408O21Rik antibody, LRRGT00105 antibody, PDZ domain containing 9 antibody, PDZD9 antibody, Pdzd9 antibody
    背景

    Synonyms: PDZ domain containing 9, PDZ domain containing protein 9, PDZD 9, PDZK-9.\, PDZD9_HUMAN.

    Background: PDZD9 (PDZ domain containing 9) is a 264 amino acid protein that contains one PDZ (DHR) domain and participates in protein binding. Conserved in chimpanzee, dog, cow, mouse and rat, PDZD9 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 16p12.1. Chromosome 16 encodes over 900 genes, approximately 90 million base pairs, makes up nearly 3 % of human cellular DNA and is associated with a variety of genetic disorders. Giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth, and the rare disorder Rubinstein-Taybi syndrome, characterized by mental retardation and predisposition to tumor growth and white blood cell neoplasias, are associated with chromosome 16. Crohn's disease, a gastrointestinal inflammatory condition, and systemic lupus erythematosis are also associated with chromosome 16.

    基因ID
    255762
    UniProt
    Q8IXQ8
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