Acad8 Protein (Myc-DYKDDDDK Tag)
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- Target See all Acad8 Proteins
- Acad8 (Acyl-CoA Dehydrogenase Family, Member 8 (Acad8))
- Protein Type
- Recombinant
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This Acad8 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human ACAD8 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 Acad8 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
- Acad8 (Acyl-CoA Dehydrogenase Family, Member 8 (Acad8))
- Alternative Name
- Acad8 (Acad8 Products)
- Synonyms
- zgc:55874 Protein, DDBDRAFT_0219367 Protein, DDBDRAFT_0237710 Protein, DDB_0219367 Protein, DDB_0237710 Protein, ACAD-8 Protein, ARC42 Protein, RGD1564209 Protein, 2310016C19Rik Protein, AI786953 Protein, acyl-CoA dehydrogenase family member 8 L homeolog Protein, acyl-CoA dehydrogenase family, member 8 Protein, acyl-CoA dehydrogenase family member 8 Protein, acyl-CoA dehydrogenase Protein, acyl-Coenzyme A dehydrogenase family, member 8 Protein, acad8.L Protein, acad8 Protein, ACAD8 Protein, LOC100231097 Protein, Acad8 Protein
- Background
- This gene encodes a member of the acyl-CoA dehydrogenase family of enzymes that catalyze the dehydrogenation of acyl-CoA derivatives in the metabolism of fatty acids or branch chained amino acids. The encoded protein is a mitochondrial enzyme that functions in catabolism of the branched-chain amino acid valine. Defects in this gene are the cause of isobutyryl-CoA dehydrogenase deficiency.[provided by RefSeq, Nov 2009].
- Molecular Weight
- 44.9 kDa
- NCBI Accession
- NP_055199
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