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DFNA5 抗体

DFNA5 适用: 人, 大鼠, 小鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6571133
发货至: 中国
  • 抗原 See all DFNA5 抗体
    DFNA5 (Deafness, Autosomal Dominant 5 (DFNA5))
    适用
    • 33
    • 20
    • 18
    • 2
    • 2
    • 2
    • 1
    人, 大鼠, 小鼠
    宿主
    • 45
    • 3
    克隆类型
    • 45
    • 3
    多克隆
    标记
    • 21
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This DFNA5 antibody is un-conjugated
    应用范围
    • 36
    • 18
    • 13
    • 13
    • 11
    • 9
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human DFNA5
    亚型
    IgG
    Top Product
    Discover our top product DFNA5 Primary Antibody
  • 应用备注
    WB 1:500 - 1:2000 IHC 1:50 - 1:200
    限制
    仅限研究用
  • 浓度
    1 mg/mL
    缓冲液
    Buffer: PBS with 0.02 % sodium azide, 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
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    DFNA5 (Deafness, Autosomal Dominant 5 (DFNA5))
    别名
    DFNA5 (DFNA5 产品)
    别名
    Dfna5h antibody, fk59f08 antibody, zgc:91916 antibody, wu:fc41e05 antibody, wu:fk59f08 antibody, MGC83660 antibody, ICERE-1 antibody, 2310037D07Rik antibody, 4932441K13Rik antibody, EG14210 antibody, Fin15 antibody, gasdermin E antibody, gasdermin Eb antibody, DFNA5, deafness associated tumor suppressor antibody, gasdermin E L homeolog antibody, Gsdme antibody, gsdmeb antibody, DFNA5 antibody, gsdme.L antibody, GSDME antibody
    背景

    Synonyms: 2310037D07Rik,4932441K13Rik,Deafness,autosomal dominant 5,Deafness,autosomal dominant 5 protein,DFNA5,DFNA5 gene,DFNA5,Dfna5h,EG14210,Fin15,ICERE 1,ICERE-1,Inversely correlated with estrogen receptor expression 1,Non-syndromic hearing impairment protein 5,Nonsyndromic hearing impairment protein

    Background: Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene.

    分子量

    Observed_MW: 50kDa

    Calculated_MW: 10kDa/36kDa/54kDa

    基因ID
    1687
    UniProt
    O60443
    途径
    Sensory Perception of Sound
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