Hemoglobin Antibody (PACO25160)
- SKU:
- PACO25160
- Product type:
- Antibody
- Reactivity:
- Human
- Host Species:
- Rabbit
- Isotype:
- IgG
- Application:
- ELISA
- Application:
- WB
- Antibody type:
- Polyclonal
- Conjugation:
- Unconjugated
Frequently bought together:
Description
| Antibody Name: | Hemoglobin Antibody (PACO25160) |
| Antibody SKU: | PACO25160 |
| Size: | 50ug |
| Host Species: | Rabbit |
| Tested Applications: | ELISA, WB |
| Recommended Dilutions: | ELISA:1:2000-1:10000, WB:1:1000-1:5000 |
| Species Reactivity: | Human |
| Immunogen: | Human Hemoglobin protein (Native Protein) |
| Form: | Liquid |
| Storage Buffer: | Preservative: 0.03% Proclin 300 Constituents: 50% Glycerol, 0.01M PBS, PH 7.4 |
| Purification Method: | >95%, Protein G purified |
| Clonality: | Polyclonal |
| Isotype: | IgG |
| Conjugate: | Non-conjugated |
 | Western blot All lanes: Hemoglobin polyclonal antibody at 2µg/ml + 293T whole cell lysate Secondary Goat polyclonal to rabbit IgG at 1/15000 dilution Predicted band size: 16 kDa Observed band size: 16 kDa . |
| Background: | Hemoglobin is involved in oxygen transport from the lung to the various peripheral tissues. The α (HBA) and β (HBB) loci determine the structure of the 2 types of polypeptide chains in adult Hemoglobin. The normal adult Hemoglobin tetramer consists of two α chains and two β chains. Mutant β globin causes sickle cell anemia. Absence of β chain causes β zero thalassemia. Reduced amounts of detectable β globin causes β plus thalassemia. |
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