hHb Antikörper (HRP)

Produktnummer ABIN2175678

Der HRP-konjugierte Maus Monoklonal anti-hHb Antikörper (Klon H5A3) (ABIN2175678) detektiert spezifisch hHb in WB. Dieser Antikörper reagiert spezifisch mit Proben aus Human.

Kurzübersicht für hHb Antikörper (HRP) (ABIN2175678)

Target: hHb

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: HRP

Applikation: Western Blotting (WB)

Klon: H5A3

Produktdetails

Kreuzreaktivität: Human

Aufreinigung: Purified by Protein G.

Immunogen: human haemoglobin full length

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:300-5000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

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

Konservierungsmittel: ProClin

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

Handhabung: Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Haltbarkeit: 12 months

Antigendetails

Target: hHb

Hintergrund:

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.

Gen-ID: 3040