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The antibody against HBB was raised in rabbit using the Recombinant Human Hemoglobin subunit beta protein (1-147AA) as the immunogen. This antibody exists as a fitc conjugated isotype IgG, purified by protein G with a purity greater than 95%.
The antibody against HBB was raised in rabbit using the Recombinant Human Hemoglobin subunit beta protein (1-147AA) as the immunogen. This antibody exists as a fitc conjugated isotype IgG, purified by protein G with a purity greater than 95%.
$299.00
| Cat.No | ADC-44115A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | HBB |
| Form | Liquid | Species Reactivity | Human |
| Isotype | IgG | Storage Buffer | 0.01M PBS, 0.03% Proclin 300; Constituents: 50% Glycerol, PH 7.4 |
| Purification Method | >95%, Protein G purified | Conjugate | FITC conjugated |
| Storage | Upon receipt |
| Immunogen Description | Recombinant Human Hemoglobin subunit beta protein (1-147AA) | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | Complete sequences for the immunogen, target protein, and peptides are available upon request. | Uniprot ID | P68871 |
Uniprot Id
P68871
Target Species
Human
Target Name
HBB
Target Full Name
Hemoglobin subunit beta
Target Function
Involved in oxygen transport from the lung to the various peripheral tissues.; LVV-hemorphin-7 potentiates the activity of bradykinin, causing a decrease in blood pressure.; 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.
Target Involvement
Heinz body anemias (HEIBAN); Beta-thalassemia (B-THAL); Sickle cell anemia (SKCA); Beta-thalassemia, dominant, inclusion body type (B-THALIB)
Target Protein Families
Globin family
Target Tissue Specificity
Red blood cells.
Target Synonyms
ECYT6; CD113t-C; beta-globin; HBB
Target 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'.
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