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hHb(H5A3) Monoclonal Antibody, AbBy Fluor® 405 Conjugated

Applications

  • WB

Reactivity

  • Human
Overview
Catalog # bsm-2118M-BF405
Product Name hHb(H5A3) Monoclonal Antibody, AbBy Fluor® 405 Conjugated
Applications WB
Reactivity Human
Specifications
Conjugation AbBy Fluor® 405
Host Mouse
Source human haemoglobin full length
Clonality Monoclonal
Clone # H5A3
Isotype IgG
Concentration 1ug/ul
Purification Purified by Protein G.
Storage Buffer Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Condition Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
Target
Gene ID 3040
Synonyms Beta globin; CD113t C; CD31; Gamma 1 globin; Hb F Agamma; HBA 1; HBA 2; HBA; HBA1; HBA2; HBB; Hbb-y; HBD; Hbe1; HBG 1; HBG; HBG1; HBGA; HBGR; Hemoglobin alpha 1; Hemoglobin alpha chain; Hemoglobin alpha locus; Hemoglobin beta; Hemoglobin beta chain; Hemoglobin beta chain complex; Hemoglobin beta locus; Hemoglobin gamma 1 chain; Hemoglobin gamma A; Hemoglobin gamma A chain; Hemoglobin gamma; Hemoglobin subunit alpha; Hemoglobin subunit beta; Hemoglobin subunit gamma 1; HSGGL1; MGC126895; MGC126897 ; PRO2979.
Background Hemoglobin is involved in oxygen transport from the lung to the various peripheral tissues. The alpha (HBA) and beta (HBB) loci determine the structure of the 2 types of polypeptide chains in adult Hemoglobin. The normal adult Hemoglobin tetramer consists of two alpha chains and two beta chains. Mutant beta globin causes sickle cell anemia. Absence of beta chain causes beta zero thalassemia. Reduced amounts of detectable beta globin causes beta plus thalassemia.
Application Dilution
WB 1:300-5000