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NSJ Bioreagents

SKU:RQ6930

ALAS2 Antibody / ASB / 5-aminolevulinic acid synthase 2

ALAS2 Antibody / ASB / 5-aminolevulinic acid synthase 2

Regular price $449.00 USD
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Delta-aminolevulinate synthase 2 also known as ALAS2 is a protein that in humans is encoded by the ALAS2 gene. 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.

Specifications

Family Primary antibody
Formulation 0.5mg/ml if reconstituted with 0.2ml sterile DI water
Format Antigen affinity purified
Host Animal Rabbit
Clonality Polyclonal (rabbit origin)
Isotype Rabbit IgG
Species Reactivity Human, Mouse, Rat
Application WB, FACS, IF, Direct ELISA
Application Details Western blot: 0.5-1 ug/ml,Flow cytometry: 1-3ug/million cells,Immunofluorescence: 5ug/ml,Direct ELISA: 0.1-0.5ug/ml
Application Note Optimal dilution of the ALAS2 antibody should be determined by the researcher.
Immunogen Recombinant human protein (amino acids M1-D190) was used as the immunogen for the ALAS2 antibody.
Buffer Lyophilized from 1X PBS with 2% Trehalose
Purity Antigen affinity purified
Storage After reconstitution, the ALAS2 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
Limitation This ALAS2 antibody is available for research use only.
Uniprot # P22557
Status Available
PDF Link https://www.nsjbio.com/tds-pdf/alas2-antibody-asb-5-aminolevulinic-acid-synthase-2-rq6930
Title ALAS2 Antibody / ASB / 5-aminolevulinic acid synthase 2
Description Delta-aminolevulinate synthase 2 also known as ALAS2 is a protein that in humans is encoded by the ALAS2 gene. 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.
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