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ALDH3A2 抗体 (AA 101-200) (Biotin)

ALDH3A2 适用: 人 WB, ELISA, IHC (p), IHC (fro) 宿主: 兔 Polyclonal Biotin
产品编号 ABIN1393381
发货至: 中国
  • 抗原 See all ALDH3A2 抗体
    ALDH3A2 (Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2))
    抗原表位
    • 14
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 101-200
    适用
    • 49
    • 10
    • 9
    • 6
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    宿主
    • 33
    • 15
    • 1
    克隆类型
    • 35
    • 14
    多克隆
    标记
    • 26
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This ALDH3A2 antibody is conjugated to Biotin
    应用范围
    • 48
    • 22
    • 19
    • 13
    • 13
    • 9
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
    预测反应
    Human,Mouse,Rat
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human ALDH3A2
    亚型
    IgG
    Top Product
    Discover our top product ALDH3A2 Primary Antibody
  • 应用备注
    WB 1:300-5000
    IHC-P 1:200-400
    IHC-F 1:100-500
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 μg/μL
    缓冲液
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    储存液
    ProClin
    注意事项
    This product contains ProClin: 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 for 12 months.
    有效期
    12 months
  • 抗原
    ALDH3A2 (Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2))
    别名
    ALDH3A2 (ALDH3A2 产品)
    别名
    ALDH10 antibody, FALDH antibody, SLS antibody, AI194803 antibody, Ahd-3 antibody, Ahd-3r antibody, Ahd3 antibody, Ahd3-r antibody, Aldh4 antibody, Aldh4-r antibody, ALDH-III antibody, CG11140 antibody, CT41571 antibody, Dhap antibody, Dmel\\CG11140 antibody, l(2)03610 antibody, Aldh-III antibody, aldh3a2 antibody, wu:fc06b11 antibody, zgc:92064 antibody, ALDH3A2 antibody, aldehyde dehydrogenase 3 family member A2 antibody, aldehyde dehydrogenase family 3, subfamily A2 antibody, aldehyde dehydrogenase 3 family, member A2 antibody, Aldehyde dehydrogenase type III antibody, fatty aldehyde dehydrogenase antibody, aldehyde dehydrogenase 3 family, member A2a antibody, aldehyde dehydrogenase 3 family member A2 S homeolog antibody, aldH antibody, ALDH3A2 antibody, Aldh3a2 antibody, Aldh-III antibody, PTRG_02589 antibody, aldh3a2 antibody, aldh3a2a antibody, aldh3a2.S antibody, aldH antibody
    背景

    Synonyms: Ahd 3, Ahd 3r, Ahd3, Ahd3 r, AL3A2_HUMAN, Aldehyde dehydrogenase 10, Aldehyde dehydrogenase 3, Aldehyde dehydrogenase 3 family, member A2, Aldehyde dehydrogenase family 3 member A2, Aldehyde dehydrogenase family 3, subfamily A2, Aldehyde dehydrogenase, family 3, subfamily A, member 2, ALDH10, Aldh3, ALDH3A2, Aldh4, Aldh4 r, Aldh4r, FALDH, Fatty aldehyde dehydrogenase, FLJ20851, Microsomal aldehyde dehydrogenase, msALDH, SLS.

    Background: Aldehyde dehydrogenases (ALDHs) mediate the NADP+-dependent oxidation of aldehydes into acids and play an important role in the detoxification of alcohol-derived acetaldehyde, as well as in lipid peroxidation and in the metabolism of corticosteroids, biogenic amines and neurotransmitters. ALDH3A2 (aldehyde dehydrogenase 3 family, member A2), also known as SLS, FALDH or ALDH10, is a 485 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the endoplasmic reticulum and belongs to the aldehyde dehydrogenase family. Expressed in a variety of tissues, including liver, heart, lung, brain, kidney and placenta, ALDH3A2 catalyzes the NAD+-dependent oxidation of long-chain aliphatic aldehydes to fatty acids, a process that is necessary for detoxification and lipid metabolism. Defects in the gene encoding ALDH3A2 are the cause of Sjoegren-Larsson syndrome (SLS), an autosomal recessive neurocutaneous disorder characterized by severe mental retardation, seizures and speech defects. Multiple isoforms of ALDH3A2 exist due to alternative splicing events.

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