HBA1 antibody (AA 56-141)

Catalog No. ABIN728938

This Rabbit Polyclonal antibody specifically detects HBA1 in WB, ELISA, IHC (p), IF (cc), IF (p), IHC (fro). It exhibits reactivity toward Human.

Quick Overview for HBA1 antibody (AA 56-141) (ABIN728938)

Target: HBA1 (Hemoglobin, alpha 1 (HBA1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This HBA1 antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Product Details anti-HBA1 Antibody

Binding Specificity: AA 56-141

Cross-Reactivity: Human

Predicted Reactivity: Rat,Monkey

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human HBA1

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Expiry Date: 12 months

Target Details for HBA1

Target: HBA1 (Hemoglobin, alpha 1 (HBA1))

Alternative Name: HBA

Background:

Synonyms: Alpha globin, Alpha-globin, Beta globin, HBA1, HBA2, HBA_HUMAN, HBH, ECYT7, HBA-T3, METHBA, Hemoglobin alpha 1, Hemoglobin alpha chain, Hemoglobin alpha locus, Hemoglobin subunit alpha,

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 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.

Gene ID: 3039

UniProt: P69905