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ALDH3A1 Polyclonal Antibody

规格: / 20μL / 60μL / 120μL / 200μL
价格: / ¥420 / ¥1010 / ¥1640 / ¥2365

货号:E-AB-14534

宿主: Rabbit

反应性: H,M,R

应用: WB,IHC

  • 详情
  • Overview

    Synonyms Acetaldehyde dehydrogenase 3,AHD 4,AHD C,AHD4,AHDC,AL3A1,Aldehyde dehydrogenase 3,Aldehyde dehydrogenase 3 family member A1,Aldehyde dehydrogenase 3A1,Aldehyde dehydrogenase,Aldehyde dehydrogenase class 3,Aldehyde dehydrogenase dimeric NADP preferring,Aldehyde dehydrogenase family 3 member A1,Aldehyde dehydrogenase family 3 subfamily A1,Aldehyde dehydrogenase family 3,subfamily A,member 1,Aldehyde dehydrogenase isozyme 3,Aldehyde dehydrogenase type III,ALDH 3,ALDH 3A1,ALDH III,ALDH,stomach type,ALDH3 A1,ALDH3,ALDH3A 1,Aldh3a1,ALDHIII,dimeric NADP-preferring,MGC10406,Stomach aldehyde dehydrogenase,Tumor associated aldehyde dehydrogenase tumor ALDH,ALDH3A1抗体
    Swissprot P30838
    Source Rabbit
    Reactivity Human,Mouse,Rat
    Immunogen Recombinant protein of human ALDH3A1
    Application WB(Detection kit: E-IR-R304),IHC(Detection kit: E-IR-R213)
    Recommended dilution WB,,1:500-1:2000;IHC,,1:50-1:200;
    Concentration 0.4 mg/mL
    Clonality Polyclonal

    Properties

    Cellular localization Cytoplasm.
    Tissue specificity High levels in stomach, esophagus and lung; low level in the liver and kidney.
    Isotype IgG
    Purification Affinity purification
    Conjugation Unconjugated
    Storage instructions Store at -20℃. Avoid freeze / thaw cycles.
    Storage buffer PBS with 0.05% sodium azide, 50% glycerol, PH7.3
    Background Aldehyde dehydrogenases oxidize various aldehydes to the corresponding acids. They are involved in the detoxification of alcohol-derived acetaldehyde and in the metabolism of corticosteroids, biogenic amines, neurotransmitters, and lipid peroxidation. The enzyme encoded by this gene forms a cytoplasmic homodimer that preferentially oxidizes aromatic and medium-chain (6 carbons or more) saturated and unsaturated aldehyde substrates. It is thought to promote resistance to UV and 4-hydroxy-2-nonenal-induced oxidative damage in the cornea. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Multiple alternatively spliced variants, encoding the same protein, have been identified.
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