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DnaJ (Hsp40) Homolog, Subfamily C, Member 19 (DNAJC19) (C-Term) Peptide

DNAJC19 适用: 人 宿主: 合成 BP, WB
产品编号 ABIN975913
发货至: 中国
  • 抗原 See all DNAJC19 products
    DNAJC19 (DnaJ (Hsp40) Homolog, Subfamily C, Member 19 (DNAJC19))
    蛋白结构域
    C-Term
    宿主
    资源
    • 2
    合成
    应用范围
    Blocking Peptide (BP), Western Blotting (WB)
    序列
    LGVSPTANKG KIRDAHRRIM LLNHPDKGGS PYIAAKINEA KDLLEGQAKK
    产品特性
    This is a synthetic peptide designed for use in combination with anti-DNAJC19 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
    纯化方法
    Purified
  • 应用备注
    Each Investigator should determine their own optimal working dilution for specific applications.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    浓度
    1 mg/mL
    缓冲液
    Final peptide concentration is 1 mg/mL in PBS.
    注意事项
    Avoid repeated freeze-thaw cycles.
    储存条件
    -20 °C
    储存方法
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • 抗原
    DNAJC19 (DnaJ (Hsp40) Homolog, Subfamily C, Member 19 (DNAJC19))
    别名
    PAM18 Peptide, TIM14 Peptide, TIMM14 Peptide, 1810055D05Rik Peptide, AA959924 Peptide, Tim14 Peptide, zgc:73251 Peptide, DNAJC19 Peptide, DKFZp469M2132 Peptide, Gm15118 Peptide, RGD1560220 Peptide, DnaJ heat shock protein family (Hsp40) member C19 Peptide, DnaJ (Hsp40) homolog, subfamily C, member 19 Peptide, DnaJ heat shock protein family (Hsp40) member C19 L homeolog Peptide, Pam18p Peptide, DnaJ heat shock protein family (Hsp40) member C19, pseudogene Peptide, DNAJC19 Peptide, Dnajc19 Peptide, dnajc19 Peptide, dnajc19.L Peptide, PAM18 Peptide, Dnajc19-ps Peptide
    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). Several transcript variants, some protein-coding and some not, have been found for this gene.

    Alias Symbols: TIM14, TIMM14, PAM18

    Protein Interaction Partner: HSPA9,PAM16,PAM16,TIMM17A

    Protein Size: 116
    分子量
    13 kDa
    基因ID
    131118
    NCBI登录号
    NM_145261, NP_660304
    UniProt
    Q96DA6
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