MCCC2 Protein (Myc-DYKDDDDK Tag)
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- Target See all MCCC2 Proteins
- MCCC2 (Methylcrotonoyl-CoA Carboxylase 2 (Beta) (MCCC2))
- Protein Type
- Recombinant
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This MCCC2 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human MCCC2 protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Purity
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product MCCC2 Protein
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- Application Notes
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Comment
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Storage
- -80 °C
- Storage Comment
- 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.
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- Target
- MCCC2 (Methylcrotonoyl-CoA Carboxylase 2 (Beta) (MCCC2))
- Alternative Name
- Mccc2 (MCCC2 Products)
- Synonyms
- 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
- Background
- 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.
- Molecular Weight
- 61.2 kDa
- NCBI Accession
- NP_071415
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