Product Name: HBB Antibody
Species Reactivity: Human
Tested Applications: IHC-P, WB
Applications: For FACS starting dilution is: 1:25For WB starting dilution is: 1:2000For IHC-P starting dilution is: 1:10~50
User Note: Optimal dilutions for each application to be determined by the researcher.
Predicted Molecular Weight: 16 kDa
Immunogen: This HBB antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 80-107 amino acids from the C-terminal region of human HBB.
Host Species: Rabbit
Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.
Physical State: Liquid
CAS NO.: 1485-00-3
Product: SUN11602
Buffer: Supplied in PBS with 0.09% (W/V) sodium azide.
Concentration: 0.5 mg/ml
Storage Conditions: Store at 4˚C for three months and -20˚C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
Clonality: Polyclonal
Conjugate: Unconjugated
Alternate Names: Hemoglobin subunit beta, Beta-globin, Hemoglobin beta chain, LVV-hemorphin-7, Spinorphin, HBB
Accession NO.: P68871
Protein Ino: 56749856
Official Symbol: HBB
Geneid: 3043
Background: The alpha (HBA) and beta (HBB) loci determine thestructure of the 2 types of polypeptide chains in adult hemoglobin,Hb A. The normal adult hemoglobin tetramer consists of two alphachains and two beta chains. Mutant beta globin causes sickle cellanemia. Absence of beta chain causes beta-zero-thalassemia. Reducedamounts of detectable beta globin causes beta-plus-thalassemia. Theorder of the genes in the beta-globin cluster is 5-epsilon –gamma-G — gamma-A — delta — beta–3.
PubMed ID:http://aac.asm.org/content/21/2/344.abstract
