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ALDH3A2 Monoclonal Antibody

商品貨號(hào)： PLA005090

適應(yīng) 性： 人,小鼠,大鼠,兔

￥600元

規(guī)格：

40μL 100μL 200μL

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MSDS

說(shuō)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(lái)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(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
說(shuō)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(hào)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(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Microsome membrane ; Single-pass membrane protein . Endoplasmic reticulum membrane ; Single-pass membrane protein ; Cytoplasmic side .
組織表達(dá)： Detected in liver (at protein level).
科研貨號(hào)： 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(lái)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(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
說(shuō)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(hào)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(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Microsome membrane ; Single-pass membrane protein . Endoplasmic reticulum membrane ; Single-pass membrane protein ; Cytoplasmic side .
組織表達(dá)： Detected in liver (at protein level).
科研貨號(hào)： PLA005090

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