Hemoglobin Subunit beta anticorps

N° du produit ABIN7228854

Cet anticorps anti-Hemoglobin Subunit beta est un anticorps Lapin Polyclonal détectant Hemoglobin Subunit beta dans WB et ELISA. Adapté pour Humain.

Aperçu rapide pour Hemoglobin Subunit beta anticorps (ABIN7228854)

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

Reactivité: Humain

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: HBB Polyclonal Antibody

Specificité: The antibody detects endogenous levels of HBB protein

Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using 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 (1:500-1:2000), ELISA (1:5000-1:20000).

Commentaires:

Primary Antibody

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.

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: -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.

Détails sur Hemoglobin Subunit beta

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

Autre désignation: HBB

Sujet: Rabbit Anti-HBB Polyclonal Antibody,Hemoglobin subunit beta, Beta-globin, Hemoglobin beta chain,The 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'.,HBB

Poids moléculaire: observerd band 16kDa

ID gène: 3043

UniProt: P68871