APPLICATION
PROPERTIES
Form
Lyophilized powder
Buffer
Batch dependent (please contact us for details)
Storage
Store at -20ºC or below. After reconstitution, keep as concentrated solution. Aliquot and store at -20ºC or below. Avoid freeze-thaw cycles.
Region/Sequence
Synthetic peptide corresponding to amino acid residues near the N-terminus of Hb β-subunit conjugated to KLH.
Purity
>95%
Conjugation
Unconjugated
Note
For laboratory use only. Not for any clinical, therapeutic, or diagnostic use in humans or animals. Not for animal or human consumption.
TARGET
Synonyms
hemoglobin subunit beta , CD113t-C , ECYT6 , beta-globin
Cellular Localization
Extracellular region, Cytosol
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]
Database
Research Area
REFERENCE
There are currently no references for Hemoglobin beta C peptide (GTX04269-PEP). Be the first to share your publications with this product.
REVIEW
There are currently no reviews for Hemoglobin beta C peptide (GTX04269-PEP). Be the first to share your experience with this product.