HBB Mutant (T87Q) Human Recombinant Protein

Product Specifications

Background

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'. [provided by RefSeq, Jul 2008]

Overview

Purified mutant recombinant protein of Human hemoglobin, beta (HBB), mutation at (T87Q)

Synonyms

Beta-globin; CD113t-C; ECYT6

Gene ID

3043

Accession Number mRNA

NM_000518

Chromosomal Location

11p15.4

Expression System

HEK293

Tag

Myc-DDK

Concentration

>50 ug/mL as determined by microplate Bradford method

Purity

> 80% as determined by SDS-PAGE and Coomassie blue staining

Form

Liquid

Buffer

25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol

Molecular Weight

15.8 kDa

Storage Conditions

Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.