Aminolevulinate, delta-, Synthase 2 (ALAS2) Peptide
ALAS2
Reactivity: Human
Host: Synthetic
BP, WB
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- Target See all ALAS2 products
- ALAS2 (Aminolevulinate, delta-, Synthase 2 (ALAS2))
- Origin
- Human
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Characteristics
- This is a synthetic peptide designed for use in combination with anti-ALAS2 antibody (Catalog #: ARP41658_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- Purification
- Purified
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- Application Notes
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handling Advice
- Avoid repeated freeze-thaw cycles.
- Storage
- -20 °C
- Storage Comment
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- ALAS2 (Aminolevulinate, delta-, Synthase 2 (ALAS2))
- Synonyms
- anh1 Peptide, asb Peptide, xlsa Peptide, ALAS-E Peptide, ALASE Peptide, ANH1 Peptide, ASB Peptide, XLDPP Peptide, XLEPP Peptide, XLSA Peptide, alas-e Peptide, cb1063 Peptide, sau Peptide, sauternes Peptide, ALAS Peptide, Alas-2 Peptide, 5'-aminolevulinate synthase 2 Peptide, aminolevulinate, delta-, synthase 2 Peptide, aminolevulinic acid synthase 2, erythroid Peptide, alas2 Peptide, ALAS2 Peptide, Alas2 Peptide, alas2.L Peptide
- Background
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ALAS2 specifies an erythroid-specific mitochondrially located enzyme. The protein catalyzes the first step in the heme biosynthetic pathway. Defects in its gene cause X-linked pyridoxine-responsive sideroblastic anemia. Alternatively spliced transcript variants encoding different isoforms have been identified.The product of this gene specifies an erythroid-specific mitochondrially located enzyme. The encoded protein catalyzes the first step in the heme biosynthetic pathway. Defects in this gene cause X-linked pyridoxine-responsive sideroblastic anemia. Alternatively spliced transcript variants encoding different isoforms have been identified.
Alias Symbols: ANH1, ASB, XLSA, ALASE, XLDPP, XLEPP, ALAS-E
Protein Interaction Partner: RABGGTB,SUCLA2,SUCLA2
Protein Size: 550 - Molecular Weight
- 60 kDa
- Gene ID
- 212
- NCBI Accession
- NM_001037967, NP_001033056
- UniProt
- P22557
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