血红蛋白α1/α-Globin抗体

Quantity size:

0.2ml

Concentration:

1mg/ml血红蛋白α1/α-Globin抗体   Buffer = 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.

Background:

Hemoglobin is involved in oxygen transport from the lung to the various peripheral tissues. The alpha (HBA) and beta (HBB) loci determine the structure of the 2 types of polypeptide chains in adult Hemoglobin. The normal adult Hemoglobin tetramer consists of two alpha chains and two血红蛋白α1/α-Globin抗体 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.Involved in oxygen transport from the lung to the various peripheral tissues.

血红蛋白α1/α-Globin抗体Also known as:

Alpha 1 globin; Alpha globin; Alpha one globin; Alpha-globin; HBA_HUMAN; HBA1; HBA2; Hemoglobin alpha 1; Hemoglobin alpha 1 chain; Hemoglobin alpha 1 globin chain; Hemoglobin alpha 2; Hemoglobin alpha chain; Hemoglobin subunit alpha; MGC126895; MGC12689.

Specificity:

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Rabbit Polyclonal IgG, 血红蛋白α1/α-Globin抗体affinity purified by Protein A.

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Reacts with: Human, Rat, Monkey, .

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Immunogen: KLH conjugated synthetic peptide derived from human HBA1.

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Predicted Molecular Weight: 15kDa.

血红蛋白α1/α-Globin抗体Storage:

Shipped at 4℃, Store at -20℃ (Avoid repeated freeze/thaw cycles).

Application:

WB=1:100-500  ELISA=1:500-1000  IHC-P=1:100-500  IHC-F=1:100-500  IF=1:100-500   
Not yet tested in other applications. 
Optimal working dilutions must be determined by the end user.

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