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Aldehyde dehydrogenase 10 mouse mAb
商品货号: PLA005255
适 应 性:
WB
¥600元
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MSDS
说明书
商品描述
  • 发货日期: 7
  • 基因名称: aldh3a2
  • Human_gene_id: 224
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=224
  • Human_swiss_prot_no: P51648
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/P51648/entry
  • Mouse_swiss_prot_no: P47740
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/P47740
  • 特异性: This antibody detects endogenous levels of Aldehyde dehydrogenase 10 and does not cross-react with related proteins.
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Monoclonal, Mouse
  • 稀释: wb 1:1000
  • 纯化工艺: The antibody was affinity-purified from mouse ascites by affinity-chromatography using epitope-specific immunogen.
  • 浓度: 1 mg/ml
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 其他名称: Aldehyde dehydrogenase;Aldehyde dehydrogenase 10;Aldehyde dehydrogenase 3 family member A2;ALDH10;ALDH3A2;DKFZp686E23276;FALDH;Fatty aldehyde dehydrogenase;FLJ20851;Microsomal aldehyde dehydrogenase;OTTHUMP00000065799;OTTHUMP00000065800;OTTHUMP00000065801;SLS.
  • 实测条带: 55kD
  • 信号通路: Glycolysis / Gluconeogenesis;Ascorbate and aldarate metabolism;Fatty acid metabolism;Valine; leucine and isoleucine degradation;Lysine degradation;Arginine and proline metabolism;Histidine metabolism;Tryptophan metabolism;beta-Alanine metabolism;Glycerolipid metabolism;Pyruvate metabolism;Propanoate metabolism;Butanoate metabolism;Limonene and pinene degradation;
  • 功能: catalytic activity:An aldehyde + NAD(+) + H(2)O = an acid + NADH.,disease:Defects in ALDH3A2 are the cause of Sjoegren-Larsson syndrome (SLS) [MIM:270200]. SLS is an autosomal recessive neurocutaneous disorder characterized by a combination of severe mental retardation, spastic di- or tetraplegia and congenital ichthyosis (increased keratinization). Ichthyosis is usually evident at birth, neurologic symptoms appear in the first or second year of life. Most patients have an IQ of less than 60. Additional clinical features include glistening white spots on the retina, seizures, short stature and speech defects.,function:Catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acids. Active on a variety of saturated and unsaturated aliphatic aldehydes between 6 and 24 carbons in length.,similarity:Belongs to the aldehyde dehydrogenase family.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Microsome membrane ; Single-pass membrane protein . Endoplasmic reticulum membrane ; Single-pass membrane protein ; Cytoplasmic side .
  • 组织表达: Detected in liver (at protein level).
  • 科研货号: PLA005255
Aldehyde dehydrogenase 10 mouse mAb
Catalog No PLA005255
Product information
  • 发货日期: 7
  • 基因名称: aldh3a2
  • Human_gene_id: 224
  • Human_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=224
  • Human_swiss_prot_no: P51648
  • Human_swiss_link: http://www.uniprot.org/uniprotkb/P51648/entry
  • Mouse_swiss_prot_no: P47740
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/P47740
  • 特异性: This antibody detects endogenous levels of Aldehyde dehydrogenase 10 and does not cross-react with related proteins.
  • 组成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 来源: Monoclonal, Mouse
  • 稀释: wb 1:1000
  • 纯化工艺: The antibody was affinity-purified from mouse ascites by affinity-chromatography using epitope-specific immunogen.
  • 浓度: 1 mg/ml
  • 储存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 说明书: 1
  • Msds: MSDS_Antibody.pdf
  • 其他名称: Aldehyde dehydrogenase;Aldehyde dehydrogenase 10;Aldehyde dehydrogenase 3 family member A2;ALDH10;ALDH3A2;DKFZp686E23276;FALDH;Fatty aldehyde dehydrogenase;FLJ20851;Microsomal aldehyde dehydrogenase;OTTHUMP00000065799;OTTHUMP00000065800;OTTHUMP00000065801;SLS.
  • 实测条带: 55kD
  • 信号通路: Glycolysis / Gluconeogenesis;Ascorbate and aldarate metabolism;Fatty acid metabolism;Valine; leucine and isoleucine degradation;Lysine degradation;Arginine and proline metabolism;Histidine metabolism;Tryptophan metabolism;beta-Alanine metabolism;Glycerolipid metabolism;Pyruvate metabolism;Propanoate metabolism;Butanoate metabolism;Limonene and pinene degradation;
  • 功能: catalytic activity:An aldehyde + NAD(+) + H(2)O = an acid + NADH.,disease:Defects in ALDH3A2 are the cause of Sjoegren-Larsson syndrome (SLS) [MIM:270200]. SLS is an autosomal recessive neurocutaneous disorder characterized by a combination of severe mental retardation, spastic di- or tetraplegia and congenital ichthyosis (increased keratinization). Ichthyosis is usually evident at birth, neurologic symptoms appear in the first or second year of life. Most patients have an IQ of less than 60. Additional clinical features include glistening white spots on the retina, seizures, short stature and speech defects.,function:Catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acids. Active on a variety of saturated and unsaturated aliphatic aldehydes between 6 and 24 carbons in length.,similarity:Belongs to the aldehyde dehydrogenase family.,
  • 相关产品: RS0001,RS0002,YM3028,YM3029
  • 细胞定位: Microsome membrane ; Single-pass membrane protein . Endoplasmic reticulum membrane ; Single-pass membrane protein ; Cytoplasmic side .
  • 组织表达: Detected in liver (at protein level).
  • 科研货号: PLA005255
  • Hunan UPT Biotechnology Co.,Ltd
    Website:www.uptbio.com Servive hotline :4006916686
    E-mail:service@uptbio.com
    Address:
    Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.
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