Full Product Name
MCCC1 (MCCA, Methylcrotonoyl-CoA Carboxylase Subunit alpha, Mitochondrial, 3-methylcrotonyl-CoA Carboxylase 1, 3-methylcrotonyl-CoA Carboxylase Biotin-containing Subunit, 3-methylcrotonyl-CoA:carbon Dioxide Ligase Subunit alpha, DKFZp686B20267, FLJ25545,
Product Synonym Names
Anti -MCCC1 (MCCA, Methylcrotonoyl-CoA Carboxylase Subunit alpha, Mitochondrial, 3-methylcrotonyl-CoA Carboxylase 1, 3-methylcrotonyl-CoA Carboxylase Biotin-containing Subunit, 3-methylcrotonyl-CoA:carbon Dioxide Ligase Subunit alpha, DKFZp686B20267, FLJ25545,
Product Gene Name
anti-MCCC1 antibody
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Immunogen Sequence
FTLQAHDQFS PFSSSSGRRL NISYTRNMTL KDGKNNVAIA VTYNHDGSYS MQIEDKTFQV LGNLYSEGDC TYLKCSVNGV ASKAKLIILE NTIYLFSKEG
Chromosome Location
Chromosome: 3; NC_000003.11 (182733006..182817373, complement). Location: 3q27
3D Structure
ModBase 3D Structure for Q96RQ3
Specificity
Recognizes human MCCC1.
Purity/Purification
Affinity Purified
Purified by Protein A affinity chromatography.
Form/Format
Supplied as a liquid in PBS, pH 7.2.
Immunogen
Partial recombinant corresponding to aa526-626 from human MCCC1 (NP_064551) with GST tag. MW of the GST tag alone is 26kD.
Preparation and Storage
May be stored at 4 degree C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20 degree C. Aliquots are stable for at least 12 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Other Notes
Small volumes of anti-MCCC1 antibody vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
anti-MCCC1 antibody
MCCC1 is the large subunit of 3-methylcrotonyl-CoA carboxylase. This enzyme functions as a heterodimer and catalyzes the carboxylation of 3-methylcrotonyl-CoA to form 3-methylglutaconyl-CoA.
Product Categories/Family for anti-MCCC1 antibody
Antibodies; Abs to Enzymes
Applications Tested/Suitable for anti-MCCC1 antibody
ELISA (EL/EIA), Western Blot (WB)
Application Notes for anti-MCCC1 antibody
Suitable for use in ELISA and Western Blot.
NCBI/Uniprot data below describe general gene information for MCCC1. It may not necessarily be applicable to this product.
NCBI Accession #
NP_064551.3
[Other Products]
NCBI GenBank Nucleotide #
NM_020166.3
[Other Products]
UniProt Primary Accession #
Q96RQ3
[Other Products]
UniProt Secondary Accession #
Q59ES4; Q9H959; Q9NS97[Other Products]
UniProt Related Accession #
Q96RQ3[Other Products]
Molecular Weight
80,473 Da[Similar Products]
NCBI Official Full Name
methylcrotonoyl-CoA carboxylase subunit alpha, mitochondrial
NCBI Official Synonym Full Names
methylcrotonoyl-CoA carboxylase 1 (alpha)
NCBI Official Symbol
MCCC1??[Similar Products]
NCBI Official Synonym Symbols
MCCA; MCC-B
??[Similar Products]
NCBI Protein Information
methylcrotonoyl-CoA carboxylase subunit alpha, mitochondrial; MCCase subunit alpha; 3-methylcrotonyl-CoA carboxylase 1; methylcrotonoyl-Coenzyme A carboxylase 1 (alpha); 3-methylcrotonyl-CoA:carbon dioxide ligase subunit alpha; 3-methylcrotonyl-CoA carboxylase biotin-containing subunit
UniProt Protein Name
Methylcrotonoyl-CoA carboxylase subunit alpha, mitochondrial
UniProt Synonym Protein Names
3-methylcrotonyl-CoA carboxylase 1; 3-methylcrotonyl-CoA carboxylase biotin-containing subunit; 3-methylcrotonyl-CoA:carbon dioxide ligase subunit alpha
UniProt Gene Name
MCCC1??[Similar Products]
UniProt Synonym Gene Names
MCCA; MCCase subunit alpha??[Similar Products]
UniProt Entry Name
MCCA_HUMAN
NCBI Summary for MCCC1
This gene encodes the large subunit of 3-methylcrotonyl-CoA carboxylase. This enzyme functions as a heterodimer and catalyzes the carboxylation of 3-methylcrotonyl-CoA to form 3-methylglutaconyl-CoA. Mutations in this gene are associated with 3-Methylcrotonylglycinuria, an autosomal recessive disorder of leucine catabolism. [provided by RefSeq, Jul 2008]
UniProt Comments for MCCC1
MCCC1: Defects in MCCC1 are the cause of methylcrotonoyl-CoA carboxylase 1 deficiency (MCC1D). An autosomal recessive disorder of leucine catabolism. The phenotype is variable, ranging from neonatal onset with severe neurological involvement to asymptomatic *****s. There is a characteristic organic aciduria with massive excretion of 3-hydroxyisovaleric acid and 3-methylcrotonylglycine, usually in combination with a severe secondary carnitine deficiency.
Protein type: Mitochondrial; Ligase; Amino Acid Metabolism - valine, leucine and isoleucine degradation; EC 6.4.1.4
Chromosomal Location of Human Ortholog: 3q27
Cellular Component: mitochondrion; mitochondrial matrix; mitochondrial inner membrane; cytosol
Molecular Function: protein binding; methylcrotonoyl-CoA carboxylase activity; metal ion binding; biotin carboxylase activity; biotin binding; ATP binding
Biological Process: vitamin metabolic process; leucine catabolic process; branched chain family amino acid catabolic process; water-soluble vitamin metabolic process; biotin metabolic process
Disease: 3-methylcrotonyl-coa Carboxylase 1 Deficiency
Research Articles on MCCC1
1. 3-methylcrotonyl-CoA carboxylase inhibition has a role in increased excretion of 3-hydroxyisovaleric acid in valproate-treated patients
Precautions
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Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.
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