Hemoglobin Alpha 1 + 2 (HBA1,HBA2) (C-Term) Antikörper (Fluoro594)

Produktnummer ABIN7996884

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch Hemoglobin Alpha 1 + 2 in FACS. Es zeigt Reaktivität gegenüber Proben von Human und Maus.

Kurzübersicht für Hemoglobin Alpha 1 + 2 (HBA1,HBA2) (C-Term) Antikörper (Fluoro594) (ABIN7996884)

Target: Hemoglobin Alpha 1 + 2 (HBA1,HBA2)

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Fluoro594

Applikation: Flow Cytometry (FACS)

Produktdetails

Bindungsspezifität: C-Term

Verwendungszweck: Anti-Hemoglobin/HBA1/HBA2 Antibody Fluoro594 Conjugated

Kreuzreaktivität (Details): No cross-reactivity with other proteins

Homologie: identical to the related mouse,rat sequences.

Aufreinigung: Immunogen affinity purified.

Immunogen: A synthetic peptide corresponding to a sequence at the C-terminus of human Hemoglobin/HBA1/HBA2, identical to the related mouse and rat sequences.

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Flow Cytometry, Optimal dilutions should be determined by end users.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Haltbarkeit: 12 months

Antigendetails

Target: Hemoglobin Alpha 1 + 2 (HBA1,HBA2)

Andere Bezeichnung: HBA1/HBA2

Hintergrund:

Background: The human alpha globin gene cluster 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.

Gene Full Name: hemoglobin subunit alpha 1

Gen-ID: 3039, 3040

UniProt: P69905