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Rabbit Anti-OXCT1 Antibody (CSB-PA017306ESR1HU)
Supplier: CUSABIO BIOTECH CO.
3-oxoacid CoA-transferase 1 Antibody,Somatic-type succinyl-CoA:3-oxoacid CoA-transferase Antibody, SCOT-s Antibody,OXCT1 Antibody,OXCT Antibody, SCOT AntibodyMore alternative names for the antibody
3 oxoacid CoA transferase 1 antibody|3-oxoacid CoA-transferase 1 antibody|EC 188.8.131.52 antibody|OTTHUMP00000120012 antibody|OTTHUMP00000221550 antibody|OXCT antibody|Oxct1 antibody|SCOT antibody|Scot S antibody|Scot-S antibody|SCOT1_HUMAN antibody|Somatic type succinyl CoA:3 oxoacid CoA transferase antibody|Somatic-type succinyl-CoA:3-oxoacid CoA-transferase antibody|Succinyl CoA:3 ketoacid CoA transferase antibody|Succinyl CoA:3 ketoacid coenzyme A transferase 1 mitochondrial antibody|Succinyl CoA:3 oxoacid CoA transferase antibody|Succinyl-CoA:3-ketoacid coenzyme A transferase 1, mitochondrial antibody
Anti-OXCT1 antibody (ab105320)
Anti-OXCT1 antibody (ab105320)
Recommended applications: ELISA, WB
Recommended dilution: Recommended dilution:WB:1:500-5000
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human Succinyl-CoA:3-ketoacid coenzyme A transferase 1, mitochondrial protein (261-520AA)
|Recommended dilution|| |
|Molecular weight|| |
Antigen Affinity Purified
Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.
|Database links|| |
Entrez Gene:5019( Human), Entrez Gene:67041( Mouse), Entrez Gene:690163( Rat), Omim:601424( Human), SwissProt:P55809( Human), SwissProt:Q9D0K2( Mouse), SwissProt:B2GV06( Rat), Unigene:278277( Human), Unigene:13445( Mouse), Unigene:98472( Rat)
|Protein 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.
|Protein 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.
|Involvement in disease|| |
Succinyl-CoA:3-oxoacid CoA transferase deficiency (SCOTD) [MIM:245050]: A disorder of ketone body metabolism, characterized by episodic ketoacidosis. Patients are usually asymptomatic between episodes. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the 3-oxoacid CoA-transferase family.
|Protein cellular localization|| |
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CUSABIO BIOTECH CO.
|Product type|| |
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