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PCDH15 抗体

PCDH15 适用: 人, 大鼠 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7118102
发货至: 中国
  • 抗原 See all PCDH15 抗体
    PCDH15 (Protocadherin-15 (PCDH15))
    适用
    • 13
    • 6
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    人, 大鼠
    宿主
    • 10
    • 3
    • 2
    克隆类型
    • 13
    • 2
    多克隆
    标记
    • 15
    This PCDH15 antibody is un-conjugated
    应用范围
    • 13
    • 6
    • 5
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC), ELISA
    纯化方法
    Immunogen affinity purified
    纯度
    ≥95 % as determined by SDS-PAGE
    免疫原
    PCDH15
    亚型
    IgG
    Top Product
    Discover our top product PCDH15 Primary Antibody
  • 应用备注
    IHC: 1:20-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,
    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
    储存方法
    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)
    有效期
    12 months
  • 抗原
    PCDH15 (Protocadherin-15 (PCDH15))
    别名
    PCDH15 (PCDH15 产品)
    别名
    CDHR15 antibody, DFNB23 antibody, USH1F antibody, BB078305 antibody, ENSMUSG00000046980 antibody, Gm9815 antibody, Ush1f antibody, av antibody, nmf19 antibody, protocadherin-15 antibody, protocadherin related 15 antibody, protocadherin-15 antibody, protocadherin 15 antibody, PCDH15 antibody, CpipJ_CPIJ005081 antibody, Pcdh15 antibody
    背景
    Synonyms:CDHR15, DFNB23, USH1F, PCD15 Background:This gene is a member of the cadherin superfamily. Family members encode integral membrane proteins that mediate calcium-dependent cell-cell adhesion. It plays an essential role in maintenance of normal retinal and cochlear function. Mutations in this gene result in hearing loss and Usher Syndrome Type IF (USH1F). Extensive alternative splicing resulting in multiple isoforms has been observed in the mouse ortholog. Similar alternatively spliced transcripts are inferred to occur in human, and additional variants are likely to occur.
    分子量
    100kDa
    基因ID
    65217
    UniProt
    Q96QU1
    途径
    Sensory Perception of Sound
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