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Email: info@nsjbio.com
- Tel: 858.663.9055
- Email: info@nsjbio.com
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ALAS2 Antibody / Erythroid Heme Biosynthesis Enzyme Antibody detects ALAS2 (5-Aminolevulinate Synthase 2), an erythroid-specific mitochondrial enzyme that catalyzes the first and rate-limiting step of heme biosynthesis. ALAS2 converts glycine and succinyl-CoA into 5-aminolevulinic acid, initiating the multistep pathway that ultimately generates heme, an essential component of hemoglobin and numerous heme-containing proteins. Because erythroid cells require large quantities of heme to support hemoglobin synthesis, ALAS2 serves as a critical regulator of red blood cell development and oxygen transport capacity. ALAS2 Antibody is widely utilized for studies of erythropoiesis, hematopoiesis, iron metabolism, and heme biosynthesis.
Expression of ALAS2 is tightly regulated during erythroid differentiation and is largely restricted to developing erythroblasts and maturing red blood cell precursors. As hematopoietic progenitor cells commit to the erythroid lineage, ALAS2 expression increases substantially to meet the metabolic demands of hemoglobin production. The resulting heme synthesis supports assembly of functional hemoglobin complexes that are required for oxygen transport throughout the body. Because of this highly specialized role, ALAS2 is frequently used as a marker of erythroid maturation and red blood cell lineage development.
ALAS2 occupies a central position within the heme biosynthetic pathway and serves as a key point of integration between iron availability, erythropoietic signaling, and hemoglobin production. Multiple regulatory mechanisms coordinate ALAS2 expression and activity to ensure balanced heme synthesis and prevent accumulation of potentially toxic metabolic intermediates. Through these functions, ALAS2 contributes to maintenance of normal erythrocyte physiology and efficient oxygen delivery within vertebrate organisms.
Disruption of ALAS2 activity has been associated with inherited and acquired disorders of erythropoiesis. Mutations affecting ALAS2 can impair heme production and contribute to abnormalities in red blood cell maturation and function. Consequently, ALAS2 has become an important target in studies of hematologic disease, iron utilization, and mechanisms regulating erythroid differentiation. Researchers frequently utilize ALAS2 Antibody to investigate pathways governing heme metabolism, erythroid development, and red blood cell biology.
Beyond its role in hematology, ALAS2 serves as an important model for understanding the relationship between cellular metabolism and lineage-specific differentiation. The enzyme links mitochondrial metabolic pathways with erythroid gene expression programs that drive hemoglobin synthesis and red blood cell maturation. Analysis of ALAS2 expression provides valuable insight into developmental hematopoiesis, iron homeostasis, and molecular mechanisms controlling erythroid lineage commitment.
ALAS2 Antibody / Erythroid Heme Biosynthesis Enzyme Antibody is useful for researchers studying erythropoiesis, hematopoiesis, heme biosynthesis, hemoglobin production, iron metabolism, red blood cell development, mitochondrial metabolism, hematologic disorders, and erythroid differentiation. Validation may include immunohistochemistry, western blotting, immunofluorescence, flow cytometry, and related protein expression applications when supported by experimental data.
Explore our Metabolism Antibodies page for additional markers involved in heme biosynthesis, iron metabolism, mitochondrial function, cellular energy pathways, and metabolic regulation.
Optimal dilution of the ALAS2 Antibody / Erythroid Heme Biosynthesis Enzyme Antibody should be determined by the researcher.
Recombinant human protein (amino acids M1-D190) was used as the immunogen for the ALAS2 antibody.
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.
ALAS2 Antibody, Erythroid Heme Biosynthesis Enzyme Antibody, 5-Aminolevulinate Synthase 2 Antibody, Delta-Aminolevulinate Synthase 2 Antibody, Erythroid-Specific ALA Synthase Antibody, Hemoglobin Synthesis Enzyme Antibody
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