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Hemoglobin Antibody (PACO25660)

SKU:
PACO25660
Product Type:
Antibody
Reactivity:
Rabbit
Host Species:
Guinea pig
Isotype:
IgG
Applications:
ELISA
Antibody Type:
Polyclonal Antibody
Conjugation:
Unconjugated
€359

Description

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Hemoglobin Antibody (PACO25660)

The Hemoglobin Antibody (PAC025660) is a powerful tool for researchers studying hemoglobin, a crucial protein responsible for transporting oxygen in the blood. This polyclonal antibody, generated in rabbits, exhibits high reactivity with human samples and is optimized for Western blot applications. By targeting the hemoglobin protein, this antibody allows for precise detection and analysis in a variety of cell types, making it ideal for investigations in hematology and related fields.Hemoglobin plays a vital role in maintaining oxygen balance in the body, and abnormalities in its structure or function can lead to various health conditions such as anemia and sickle cell disease.

By studying hemoglobin using this antibody, researchers can gain valuable insights into the mechanisms underlying these disorders and develop new therapeutic strategies. Additionally, this antibody may also be useful in diagnostic applications for detecting hemoglobin-related abnormalities in clinical samples.

Antibody Name:Hemoglobin Antibody (PACO25660)
Antibody SKU:PACO25660
Size:50ug
Host Species:Guinea pig
Tested Applications:ELISA
Recommended Dilutions:
Species Reactivity:Rabbit
Immunogen:Rabbit Hemoglobin (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
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.
Synonyms:Hemoglobin

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