ALDH1A2 antibody
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- Target See all ALDH1A2 Antibodies
- ALDH1A2 (Aldehyde Dehydrogenase 1 Family, Member A2 (ALDH1A2))
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Reactivity
- Human, Mouse, Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This ALDH1A2 antibody is un-conjugated
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Application
- Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
- Characteristics
- Polyclonal Antibody
- Purification
- Affinity purification
- Immunogen
- Synthetic peptide of human ALDH1A2
- Isotype
- IgG
- Top Product
- Discover our top product ALDH1A2 Primary Antibody
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- Application Notes
- WB 1:500-1:2000, IHC 1:25-1:100
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.6 mg/mL
- Buffer
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- ALDH1A2 (Aldehyde Dehydrogenase 1 Family, Member A2 (ALDH1A2))
- Alternative Name
- ALDH1A2 (ALDH1A2 Products)
- Synonyms
- Raldh-2 antibody, RALDH(II) antibody, RALDH2 antibody, RALDH2-T antibody, fb50h01 antibody, raldh2 antibody, AV116159 antibody, Aldh1a7 antibody, Raldh1 antibody, Raldh2 antibody, aldehyde dehydrogenase 1 family, member A2 antibody, aldehyde dehydrogenase 1 family member A2 antibody, aldehyde dehydrogenase family 1, subfamily A2 antibody, Aldh1a2 antibody, ALDH1A2 antibody, aldh1a2 antibody
- Background
- This protein belongs to the aldehyde dehydrogenase family of proteins. The product of this gene is an enzyme that catalyzes the synthesis of retinoic acid (RA) from retinaldehyde. Retinoic acid, the active derivative of vitamin A (retinol), is a hormonal signaling molecule that functions in developing and adult tissues. The studies of a similar mouse gene suggest that this enzyme and the cytochrome CYP26A1, concurrently establish local embryonic retinoic acid levels which facilitate posterior organ development and prevent spina bifida. Four transcript variants encoding distinct isoforms have been identified for this gene.
- Molecular Weight
- 57 kDa
- NCBI Accession
- NP_001193826
- UniProt
- O94788
- Pathways
- Retinoic Acid Receptor Signaling Pathway
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