"HBB" Related Products

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Native Human Hemoglobin S, Ferrous Stabilized

Cat.No.: HBB-001H
Product Overview: Solubility
H2O: soluble 20 mg/mL
Suitability
Suitable for electrophoresis and chromatography standard (has not been tested for functional equivalence against native preparations (unlyophilized ferrous hemoglobins).)
Description: The alpha (HBA) and beta (HBB) loci determine the structure of the 2 types of polypeptide chains in adult hemoglobin, Hb A. 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. The order of the genes in the beta-globin cluster is 5'-epsilon -- gamma-G -- gamma-A -- delta -- beta--3'.
Species: Human
Form: Lyophilized powder
Applications: Hemoglobin S was used in the determination of fetal hemoglobin by time-resolved immunofluorometric assay.
Storage: At -20 centigrade.
Reconstitution: When reconstituted with buffer, gives >90% ferrous hemoglobin.
Gene Name: HBB
Official Symbol: HBB hemoglobin subunit beta [ Homo sapiens (human) ]
Synonyms: Sickle cell hemoglobin; HBB; hemoglobin subunit beta; CD113t-C; beta-globin; hemoglobin subunit beta; beta globin chain; hemoglobin, beta
Gene ID: 3043
mRNA Refseq: NM_000518
Protein Refseq: NP_000509
MIM: 141900
UniProt ID: P68871

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