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DNAJC19 抗体

DNAJC19 适用: 人, 小鼠, 大鼠 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7261189
发货至: 中国
  • 抗原 See all DNAJC19 抗体
    DNAJC19 (DnaJ (Hsp40) Homolog, Subfamily C, Member 19 (DNAJC19))
    适用
    • 24
    • 16
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    人, 小鼠, 大鼠
    宿主
    • 26
    • 5
    克隆类型
    • 29
    • 2
    多克隆
    标记
    • 17
    • 1
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    • 1
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    This DNAJC19 antibody is un-conjugated
    应用范围
    • 16
    • 13
    • 13
    • 9
    • 4
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Recombinant fusion protein of human DNAJC19 (NP_660304.1).
    亚型
    IgG
    Top Product
    Discover our top product DNAJC19 Primary Antibody
  • 应用备注
    WB 1:500-1:2000 IHC 1:50-1:200 IF 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 mg/mL
    缓冲液
    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
    DNAJC19 (DnaJ (Hsp40) Homolog, Subfamily C, Member 19 (DNAJC19))
    别名
    DNAJC19 (DNAJC19 产品)
    别名
    PAM18 antibody, TIM14 antibody, TIMM14 antibody, 1810055D05Rik antibody, AA959924 antibody, Tim14 antibody, zgc:73251 antibody, DNAJC19 antibody, DKFZp469M2132 antibody, Gm15118 antibody, RGD1560220 antibody, DnaJ heat shock protein family (Hsp40) member C19 antibody, DnaJ (Hsp40) homolog, subfamily C, member 19 antibody, DnaJ heat shock protein family (Hsp40) member C19 L homeolog antibody, Pam18p antibody, DnaJ heat shock protein family (Hsp40) member C19, pseudogene antibody, DNAJC19 antibody, Dnajc19 antibody, dnajc19 antibody, dnajc19.L antibody, PAM18 antibody, Dnajc19-ps antibody
    背景
    The protein encoded by this gene is thought to be part of a complex involved in the ATP-dependent transport of transit peptide-containing proteins from the inner cell membrane to the mitochondrial matrix. Defects in this gene are a cause of 3-methylglutaconic aciduria type 5 (MGA5), also known as dilated cardiomyopathy with ataxia (DCMA). Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 1, 2, 6, 10, 14 and 19.
    分子量

    Observed_MW: 12 kDa

    Calculated_MW: 10 kDa/12 kDa

    基因ID
    131118
    UniProt
    Q96DA6
    途径
    SARS-CoV-2 Protein Interactome
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