MCCC2 Protein (Myc-DYKDDDDK Tag)

N° du produit ABIN2725599

Détail du produit

Antigène: MCCC2 (Methylcrotonoyl-CoA Carboxylase 2 (Beta) (MCCC2))

Type de proteíne: Recombinant

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette MCCC2 protéine est marqué à la Myc-DYKDDDDK Tag.

Application: Antibody Production (AbP), Standard (STD)

Attributs du produit:

• Recombinant human MCCC2 protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Pureté: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Information d'application

Indications d'application: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Commentaires:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Stockage

Concentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Stock: -80 °C

Stockage commentaire: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Détail du antigène

Antigène: MCCC2 (Methylcrotonoyl-CoA Carboxylase 2 (Beta) (MCCC2))

Autre désignation: Mccc2 (MCCC2 Produits)

Synonymes: si:dkey-57m14.1 Protein, zgc:85685 Protein, MCCB Protein, 3-METHYLCROTONYL-COA CARBOXYLASE Protein, 3-methylcrotonyl-CoA carboxylase Protein, F28A23.210 Protein, F28A23_210 Protein, 4930552N12Rik Protein, methylcrotonoyl-CoA carboxylase 2 (beta) Protein, methylcrotonoyl-CoA carboxylase 2 Protein, methylcrotonoyl-CoA carboxylase 2 S homeolog Protein, 3-methylcrotonyl-CoA carboxylase Protein, methylcrotonoyl-Coenzyme A carboxylase 2 (beta) Protein, mccc2 Protein, MCCC2 Protein, mccc2.S Protein, Mccc2 Protein, MCCB Protein

Sujet: This gene encodes the small 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.

Poids moléculaire: 61.2 kDa

NCBI Accession: NP_071415