HBa2 anticorps (AA 100-128)

N° du produit ABIN653363

L’anticorps Lapin Polyclonal anti-HBa2 a été validé pour WB et FACS. Il convient pour détecter HBa2 dans des échantillons de Humain et Souris.

Aperçu rapide pour HBa2 anticorps (AA 100-128) (ABIN653363)

Antigène: HBa2 (Hemoglobin, alpha 2 (HBa2))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp HBa2 est non-conjugé

Application: Western Blotting (WB), Flow Cytometry (FACS)

Clone: RB24041

Détail du produit anti-HBa2 anticorps

Épitope: AA 100-128

Homologie: Pr

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This HBA2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 100-128 amino acids from the Central region of human HBA2.

Isotype: IgG

Information d'application

Indications d'application: WB: 1:2000. WB: 1:1000. FC: 1:25

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Agent conservateur: Sodium azide

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

Stock: 4 °C,-20 °C

Stockage commentaire: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Date de péremption: 6 months

Détails sur HBa2

Antigène: HBa2 (Hemoglobin, alpha 2 (HBa2))

Autre désignation: HBA2

Sujet: HBA2 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: 15258

ID gène: 3039

NCBI Accession: NP_000508, NP_000549

UniProt: P69905