HBA1 anticorps (AA 30-110)

N° du produit ABIN7228850

Cet anticorps Lapin Polyclonal détecte spécifiquement HBA1 dans WB et ELISA. Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour HBA1 anticorps (AA 30-110) (ABIN7228850)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp HBA1 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-HBA1 anticorps

Épitope: AA 30-110

Fonction: Rabbit Anti-HBA Polyclonal Antibody

Specificité: The antibody detects endogenous levels of HBA protein

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogène: Synthesized peptide derived from part region of human HBA protein at AA range: 30-110

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000,ELISA 1:5000-20000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA

Agent conservateur: ProClin

Précaution d'utilisation: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur HBA1

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

Autre désignation: HBA

Sujet: Alpha-globin, Hemoglobin alpha chainThe human alpha globin gene cluster located on chromosome 16 spans about 30 kb and includes seven loci: 5'-zeta-pseudozeta-mu-pseudoalpha-1-alpha-2-alpha-1-theta-3'. The alpha-2 (HBA2) and alpha-1 (HBA1) coding sequences are identical. These genes differ slightly over the 5' untranslated regions and the introns, but they differ significantly over the 3' untranslated regions. Two alpha chains plus two beta chains constitute HbA, which in normal adult life comprises about 97 % of the total hemoglobin, alpha chains combine with delta chains to constitute HbA-2, which with HbF (fetal hemoglobin) makes up the remaining 3 % of adult hemoglobin. Alpha thalassemias result from deletions of each of the alpha genes as well as deletions of both HBA2 and HBA1, some nondeletion alpha thalassemias have also been reported.

Poids moléculaire: 15kD

ID gène: 3039

UniProt: P69905