Hemoglobin Subunit beta anticorps

N° du produit ABIN7228854

Cet anticorps anti-Hemoglobin Subunit beta Polyclonal Lapin (ABIN7228854) détecte spécifiquement Hemoglobin Subunit beta dans WB et ELISA. L’anticorps est réactif avec des échantillons de Humain et Rat.

Aperçu rapide pour Hemoglobin Subunit beta anticorps (ABIN7228854)

Antigène: Hemoglobin Subunit beta (HBB) (Hemoglobin beta (HBB))

Reactivité: Humain, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Hemoglobin Subunit beta est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-Hemoglobin Subunit beta anticorps

Fonction: Rabbit Anti-HBB Polyclonal Antibody

Specificité: The antibody detects endogenous levels of HBB 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 HBB protein

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 Hemoglobin Subunit beta

Antigène: Hemoglobin Subunit beta (HBB) (Hemoglobin beta (HBB))

Autre désignation: HBB

Sujet: Hemoglobin subunit beta, Beta-globin, Hemoglobin beta chainThe alpha (HBA) and beta (HBB) loci determine the structure of the 2 types of polypeptide chains in adult hemoglobin, Hb A. 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. The order of the genes in the beta-globin cluster is 5'-epsilon -- gamma-G -- gamma-A -- delta -- beta--3'.

Poids moléculaire: 16kD

ID gène: 3043

UniProt: P68871