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MCAD Polyclonal Antibody

Polyclonal antibody

Specification

BYab-02846

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Host
Reactiveness
Use
Molecular weight (DA)
46kD
Immunogen
The antiserum was produced against synthesized peptide derived from human MCAD. AA range:134-183
Specificity
MCAD Polyclonal Antibody detects endogenous levels of MCAD protein.
Source
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Dilution rate
WB 1:500-2000;IHC-p 1:50-300
Purification process (Immunogen)
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration
1 mg/ml
Background
This gene encodes the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Defects in this gene cause medium-chain acyl-CoA dehydrogenase deficiency, a disease characterized by hepatic dysfunction, fasting hypoglycemia, and encephalopathy, which can result in infantile death. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008],
Function
catalytic activity:Acyl-CoA + acceptor = 2,3-dehydroacyl-CoA + reduced acceptor.,cofactor:FAD.,disease:Defects in ACADM are the cause of medium-chain acyl-CoA dehydrogenase deficiency (MCAD deficiency) [MIM:201450]. It is an autosomal recessive disease which causes fasting hypoglycemia, hepatic dysfunction, and encephalopathy, often resulting in death in infancy. The disease frequency is one in 13000.,function:This enzyme is specific for acyl chain lengths of 4 to 16.,miscellaneous:A number of straight-chain acyl-CoA dehydrogenases of different substrate specificities are present in mammalian tissues.,miscellaneous:Utilizes the electron transfer flavoprotein (ETF) as electron acceptor that transfers the electrons to the main mitochondrial respiratory chain via ETF-ubiquinone oxidoreductase (ETF dehydrogenase).,pathway:Lipid metabolism; mitochondrial fatty acid beta-oxidation.,similarity:
Gene Name
ACADM
Protein name
Medium-chain specific acyl-CoA dehydrogenase mitochondrial
Abbreviation
MCAD
Other name
ACADM; Medium-chain specific acyl-CoA dehydrogenase, mitochondrial; MCAD
Fields
>>Fatty acid degradation;>>Valine, leucine and isoleucine degradation;>>Metabolic pathways;>>Fatty acid metabolism;>>PPAR signaling pathway;>>Alcoholic liver disease
Human gene ID
34
Human protein sequence Database
P11310
Mouse gene ID
11364
Mouse protein sequence database
P45952
Rat gene ID
24158
Rat protein sequence database
P08503
Cellular localization
Mitochondrion matrix .
Tissue expression
Brain,Cajal-Retzius cell,Cerebellum,Colon,Liver,
Storage
-20°C/1 year

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MCAD Polyclonal Antibody

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