ALDH3B1 Protein (Myc-DYKDDDDK Tag)
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- Target See all ALDH3B1 Proteins
- ALDH3B1 (Aldehyde Dehydrogenase 3 Family, Member B1 (ALDH3B1))
- Protein Type
- Recombinant
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Origin
- Human
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Source
- HEK-293 Cells
- Purification tag / Conjugate
- This ALDH3B1 protein is labelled with Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Characteristics
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- Recombinant human ALDH4 (transcript variant P5CDhS) 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 ALDH3B1 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
- ALDH3B1 (Aldehyde Dehydrogenase 3 Family, Member B1 (ALDH3B1))
- Alternative Name
- Aldh4 (ALDH3B1 Products)
- Synonyms
- ALDH4 Protein, ALDH7 Protein, aldh4 Protein, aldh7 Protein, 1700001N19Rik Protein, aldh3d1 Protein, cb508 Protein, fb17d04 Protein, wu:fb17d04 Protein, aldehyde dehydrogenase 3 family member B1 Protein, aldehyde dehydrogenase 3 family member B1 L homeolog Protein, aldehyde dehydrogenase 3 family, member B1 Protein, aldehyde dehydrogenase family 3 member B1 Protein, ALDH3B1 Protein, aldh3b1.L Protein, Aldh3b1 Protein, LOC100548954 Protein, aldh3b1 Protein
- Background
- This protein belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene.
- Molecular Weight
- 59 kDa
- NCBI Accession
- NP_733844
- Pathways
- Monocarboxylic Acid Catabolic Process
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