电话:
+86 (0512) 65829739
传真:
+86 (010) 6788 5057
电子邮件:
orders@antibodies-online.cn

DFNA5 抗体

DFNA5 适用: 人, 大鼠, 小鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7113358
发货至: 中国
  • 抗原 See all DFNA5 抗体
    DFNA5 (Deafness, Autosomal Dominant 5 (DFNA5))
    适用
    • 30
    • 19
    • 17
    • 2
    • 2
    • 2
    • 1
    人, 大鼠, 小鼠
    宿主
    • 42
    • 3
    克隆类型
    • 44
    • 1
    多克隆
    标记
    • 18
    • 4
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This DFNA5 antibody is un-conjugated
    应用范围
    • 33
    • 17
    • 13
    • 13
    • 10
    • 9
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    纯化方法
    Immunogen affinity purified
    纯度
    ≥95 % as determined by SDS-PAGE
    免疫原
    deafness, autosomal dominant 5
    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
  • 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
    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:deafness, autosomal dominant 5, DFNA5, ICERE 1, ICERE1 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
    Refer to figures
    基因ID
    1687
    UniProt
    O60443
    途径
    Sensory Perception of Sound
You are here:
客服