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Aldehyde dehydrogenase 10 mouse mAb

商品貨號： PLA005255

適應(yīng) 性： 人

￥600元

規(guī)格：

40μL 100μL 200μL

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MSDS

說明書

商品描述

發(fā)貨日期： 7
基因名稱： 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
特異性： This antibody detects endogenous levels of Aldehyde dehydrogenase 10 and does not cross-react with related proteins.
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
純化工藝： The antibody was affinity-purified from mouse ascites by affinity-chromatography using epitope-specific immunogen.
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： 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.
實測條帶： 55kD
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(guān)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： PLA005255

Aldehyde dehydrogenase 10 mouse mAb

Catalog No PLA005255

Product information

發(fā)貨日期： 7
基因名稱： 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
特異性： This antibody detects endogenous levels of Aldehyde dehydrogenase 10 and does not cross-react with related proteins.
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
純化工藝： The antibody was affinity-purified from mouse ascites by affinity-chromatography using epitope-specific immunogen.
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： 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.
實測條帶： 55kD
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(guān)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： PLA005255

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