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SCOT1 rabbit pAb

商品貨號： PLA020782

適應(yīng) 性： 人,小鼠,大鼠

￥600元

規(guī)格：

40μL 100μL 200μL

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MSDS

說明書

商品描述

基因名稱： OXCT1 OXCT SCOT
蛋白名稱： SCOT1
Human_gene_id： 5019
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=5019
Human_swiss_prot_no： P55809
Human_swiss_link： https://www.uniprot.org/uniprotkb/P55809/entry
Mouse_gene_id： 67041
Mouse_gene_link： https://www.uniprot.org/uniprot/67041
Mouse_swiss_prot_no： Q9D0K2
Mouse_swiss_link： https://www.uniprot.org/uniprotkb/Q9D0K2
Rat_gene_id： 690163
Rat_gene_link： https://www.uniprot.org/uniprot/690163
Rat_swiss_prot_no： B2GV06
Rat_swiss_link： https://www.uniprot.org/uniprotkb/B2GV06
特異性： This antibody detects endogenous levels of SCOT1 at Human/Mouse/Rat
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Polyclonal, Rabbit,IgG
稀釋： WB 1:500-2000;IHC-p 1:50-300; ELISA 2000-20000
純化工藝： The antibody was affinity-purified from rabbit antiserum 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
分子量： 57kD
功能： catalytic activity:Succinyl-CoA + a 3-oxo acid = succinate + a 3-oxoacyl-CoA.,disease:Defects in OXCT1 are a cause of ketoacidosis [MIM:245050].,function:Key enzyme for ketone body catabolism. Transfers the CoA moiety from succinate to acetoacetate. Formation of the enzyme-CoA intermediate proceeds via an unstable anhydride species formed between the carboxylate groups of the enzyme and substrate.,pathway:Ketone metabolism; succinyl-CoA degradation; acetoacetyl-CoA from succinyl-CoA: step 1/1.,similarity:Belongs to the 3-oxoacid CoA-transferase family.,subunit:Homodimer.,tissue specificity:Abundant in heart, followed in order by kidney, brain, and muscle, whereas in liver it is undetectable; also detectable in leukocytes and fibroblasts.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Mitochondrion .
組織表達(dá)： Abundant in heart, followed in order by brain, kidney, skeletal muscle, and lung, whereas in liver it is undetectable. Expressed (at protein level) in all tissues (except in liver), most abundant in myocardium, then brain, kidney, adrenal glands, skeletal muscle and lung; also detectable in leukocytes and fibroblasts.
科研貨號： PLA020782

SCOT1 rabbit pAb

Catalog No PLA020782

Product information

基因名稱： OXCT1 OXCT SCOT
蛋白名稱： SCOT1
Human_gene_id： 5019
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=5019
Human_swiss_prot_no： P55809
Human_swiss_link： https://www.uniprot.org/uniprotkb/P55809/entry
Mouse_gene_id： 67041
Mouse_gene_link： https://www.uniprot.org/uniprot/67041
Mouse_swiss_prot_no： Q9D0K2
Mouse_swiss_link： https://www.uniprot.org/uniprotkb/Q9D0K2
Rat_gene_id： 690163
Rat_gene_link： https://www.uniprot.org/uniprot/690163
Rat_swiss_prot_no： B2GV06
Rat_swiss_link： https://www.uniprot.org/uniprotkb/B2GV06
特異性： This antibody detects endogenous levels of SCOT1 at Human/Mouse/Rat
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Polyclonal, Rabbit,IgG
稀釋： WB 1:500-2000;IHC-p 1:50-300; ELISA 2000-20000
純化工藝： The antibody was affinity-purified from rabbit antiserum 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
分子量： 57kD
功能： catalytic activity:Succinyl-CoA + a 3-oxo acid = succinate + a 3-oxoacyl-CoA.,disease:Defects in OXCT1 are a cause of ketoacidosis [MIM:245050].,function:Key enzyme for ketone body catabolism. Transfers the CoA moiety from succinate to acetoacetate. Formation of the enzyme-CoA intermediate proceeds via an unstable anhydride species formed between the carboxylate groups of the enzyme and substrate.,pathway:Ketone metabolism; succinyl-CoA degradation; acetoacetyl-CoA from succinyl-CoA: step 1/1.,similarity:Belongs to the 3-oxoacid CoA-transferase family.,subunit:Homodimer.,tissue specificity:Abundant in heart, followed in order by kidney, brain, and muscle, whereas in liver it is undetectable; also detectable in leukocytes and fibroblasts.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Mitochondrion .
組織表達(dá)： Abundant in heart, followed in order by brain, kidney, skeletal muscle, and lung, whereas in liver it is undetectable. Expressed (at protein level) in all tissues (except in liver), most abundant in myocardium, then brain, kidney, adrenal glands, skeletal muscle and lung; also detectable in leukocytes and fibroblasts.
科研貨號： PLA020782

Hunan UPT Biotechnology Co.,Ltd

Website：m.tjdqdt.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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