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Aldehyde Dehydrogenase 4 Family, Member A1 (ALDH4A1) Peptide

ALDH4A1 适用: 人 宿主: 合成 BP, WB, IHC
产品编号 ABIN973113
发货至: 中国
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Quick Overview for Aldehyde Dehydrogenase 4 Family, Member A1 (ALDH4A1) Peptide (ABIN973113)

抗原

ALDH4A1 (Aldehyde Dehydrogenase 4 Family, Member A1 (ALDH4A1))

宿主

资源

  • 6
合成

应用范围

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • 产品特性

    This is a synthetic peptide designed for use in combination with anti-ALDH4A1 antibody (Catalog #: ARP45697_T100). 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

    ALDH4A1 (Aldehyde Dehydrogenase 4 Family, Member A1 (ALDH4A1))

    背景

    ALDH4A1 belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline.This protein belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline. Two transcript variants encoding the same protein have been identified for this gene.

    Alias Symbols: ALDH4, P5CD, P5CDh, P5CDhL, P5CDhS

    Protein Size: 563

    分子量

    62 kDa

    基因ID

    8659

    NCBI登录号

    NM_003748, NP_003739

    UniProt

    P30038
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