HBB Antibody (C-term)
Peptide Affinity Purified Rabbit Polyclonal Antibody (Pab)
|Application ||WB, E|
|Other Accession||P04246, P02101, P02128, P06643, P06642, P02042, P02057, P02112, P02081, P11517, P02089, P02091, P02088, NP_000509.1, P68056, P02083, P02062, P02075|
|Predicted||Mouse, Rat, Sheep, Bovine, Chicken, Horse, Rabbit, Pig|
|Calculated MW||H=16 KDa|
|Antigen Region||80-107 aa|
|Other Names||HBB; Hemoglobin subunit beta; Beta-globin; Hemoglobin beta chain; LVV-hemorphin-7|
|Target/Specificity||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.|
|Format||Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.|
|Storage||Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.|
|Precautions||HBB Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures.|
|Function||Involved in oxygen transport from the lung to the various peripheral tissues. Spinorphin: functions as an endogenous inhibitor of enkephalin-degrading enzymes such as DPP3, and as a selective antagonist of the P2RX3 receptor which is involved in pain signaling, these properties implicate it as a regulator of pain and inflammation.|
|Tissue Location||Red blood cells..|
Thousands of laboratories across the world have published research that depended on the performance of antibodies from Abgent to advance their research. Check out links to articles that cite our products in major peer-reviewed journals, organized by research category.
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Provided below are standard protocols that you may find useful for product applications.
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'.
Bailey, S.D., et al. Diabetes Care 33(10):2250-2253(2010)
Zhou, D., et al. Nat. Genet. 42(9):742-744(2010)
Onakoya, P.A., et al. Ear Nose Throat J 89(7):306-310(2010)
Belisario, A.R., et al. Acta Haematol. 124(3):162-170(2010)
Prakobkaew, N., et al. Acta Haematol. 124(2):115-119(2010)
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