HBA1 anticorps (Middle Region)

N° du produit ABIN952707

Cet anticorps anti-HBA1 est un anticorps Lapin Polyclonal détectant HBA1 dans WB, IHC (p), FACS et EIA. Adapté pour Humain et Souris.

Aperçu rapide pour HBA1 anticorps (Middle Region) (ABIN952707)

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

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp HBA1 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS), Enzyme Immunoassay (EIA)

Détail du produit anti-HBA1 anticorps

Épitope: AA 107-136, Middle Region

Specificité: This antibody recognizes Human and Mouse Hemoglobin alpha (Center).

Purification: Protein A column, followed by peptide affinity purification

Immunogène: KLH conjugated synthetic peptide between 107~136 amino acids from the Central region of human Hemoglobin alpha Genename: HBA2, HBA1

Isotype: Ig Fraction

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS containing 0.09 % (W/V) Sodium Azide as preservative

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.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Détails sur HBA1

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

Autre désignation: Hemoglobin alpha

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.Synonyms: Alpha-globin, HBA1, Hemoglobin alpha chain

Poids moléculaire: 15258 Da

ID gène: 3039

NCBI Accession: NP_000508