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首頁 > 抗體 > 一抗 > 其它 > ALDH3A2 Monoclonal Antibody
ALDH3A2 Monoclonal Antibody
商品貨號: PLA005090
適 應 性: 人,小鼠,大鼠,兔
WB
¥600元
規(guī)格:
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MSDS
說明書
商品描述
  • 發(fā)貨日期: 7
  • 基因名稱: ALDH3A2
  • 蛋白名稱: Fatty aldehyde dehydrogenase
  • 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_gene_id: 11671
  • Mouse_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=11671
  • Mouse_swiss_prot_no: P47740
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/P47740
  • Rat_gene_id: 65183
  • Rat_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=65183
  • Rat_swiss_prot_no: P30839
  • Rat_swiss_link: http://www.uniprot.org/uniprot/P30839
  • 特異性: ALDH3A2 Monoclonal Antibody detects endogenous levels of ALDH3A2 protein.
  • 組成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 來源: Monoclonal, Mouse
  • 稀釋: WB 1:1000 - 1:2000. Not yet tested in other applications.
  • 純化工藝: Affinity purification
  • 濃度: 1 mg/ml
  • 儲存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 說明書: 1
  • Msds: MSDS_Antibody.pdf
  • 其他名稱: ALDH3A2; ALDH10; FALDH; Fatty aldehyde dehydrogenase; Aldehyde dehydrogenase 10; Aldehyde dehydrogenase family 3 member A2; Microsomal aldehyde dehydrogenase
  • 信號通路: 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.,
  • 相關產(chǎn)品: RS0001,RS0002,YM3028,YM3029
  • 細胞定位: Microsome membrane ; Single-pass membrane protein . Endoplasmic reticulum membrane ; Single-pass membrane protein ; Cytoplasmic side .
  • 組織表達: Detected in liver (at protein level).
  • 科研貨號: PLA005090
ALDH3A2 Monoclonal Antibody
Catalog No PLA005090
Product information
  • 發(fā)貨日期: 7
  • 基因名稱: ALDH3A2
  • 蛋白名稱: Fatty aldehyde dehydrogenase
  • 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_gene_id: 11671
  • Mouse_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=11671
  • Mouse_swiss_prot_no: P47740
  • Mouse_swiss_link: http://www.uniprot.org/uniprot/P47740
  • Rat_gene_id: 65183
  • Rat_gene_link: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=65183
  • Rat_swiss_prot_no: P30839
  • Rat_swiss_link: http://www.uniprot.org/uniprot/P30839
  • 特異性: ALDH3A2 Monoclonal Antibody detects endogenous levels of ALDH3A2 protein.
  • 組成: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 來源: Monoclonal, Mouse
  • 稀釋: WB 1:1000 - 1:2000. Not yet tested in other applications.
  • 純化工藝: Affinity purification
  • 濃度: 1 mg/ml
  • 儲存: -15°C to -25°C/1 year(Do not lower than -25°C)
  • 說明書: 1
  • Msds: MSDS_Antibody.pdf
  • 其他名稱: ALDH3A2; ALDH10; FALDH; Fatty aldehyde dehydrogenase; Aldehyde dehydrogenase 10; Aldehyde dehydrogenase family 3 member A2; Microsomal aldehyde dehydrogenase
  • 信號通路: 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.,
  • 相關產(chǎn)品: RS0001,RS0002,YM3028,YM3029
  • 細胞定位: Microsome membrane ; Single-pass membrane protein . Endoplasmic reticulum membrane ; Single-pass membrane protein ; Cytoplasmic side .
  • 組織表達: Detected in liver (at protein level).
  • 科研貨號: PLA005090
  • Hunan UPT Biotechnology Co.,Ltd
    Website:m.jx3dscan.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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