hHb anticorps (HRP)

N° du produit ABIN2175678

Détail du produit

Antigène: hHb

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: HRP

Application: Western Blotting (WB)

Réactivité croisée: Humain

Purification: Purified by Protein G.

Immunogène: human haemoglobin full length

Clone: H5A3

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

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

Conseil sur la manipulation: Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détail du antigène

Antigène: hHb

Sujet:

Synonyms: Beta globin, CD113t C, CD31, Gamma 1 globin, Hb F Agamma, HBA 1, HBA 2, HBA, HBA1, HBA2, HBB, Hbb-y, HBD, Hbe1, HBG 1, HBG, HBG1, HBGA, HBGR, Hemoglobin alpha 1, Hemoglobin alpha chain, Hemoglobin alpha locus, Hemoglobin beta, Hemoglobin beta chain, Hemoglobin beta chain complex, Hemoglobin beta locus, Hemoglobin gamma 1 chain, Hemoglobin gamma A, Hemoglobin gamma A chain, Hemoglobin gamma, Hemoglobin subunit alpha, Hemoglobin subunit beta, Hemoglobin subunit gamma 1, HSGGL1, MGC126895, MGC126897 , PRO2979.

Background: Hemoglobin is involved in oxygen transport from the lung to the various peripheral tissues. The alpha (HBA) and beta (HBB) loci determine the structure of the 2 types of polypeptide chains in adult Hemoglobin. 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.

ID gène: 3040