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SPTA1 Antikörper

Der Kaninchen Monoklonal Anti-SPTA1-Antikörper wurde für WB validiert. Er ist geeignet, SPTA1 in Proben von Human zu detektieren.
Produktnummer ABIN7270517

Kurzübersicht für SPTA1 Antikörper (ABIN7270517)

Target

Alle SPTA1 Antikörper anzeigen
SPTA1 (Spectrin alpha 1, Erythrocytic (SPTA1))

Reaktivität

  • 67
  • 13
  • 5
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 39
  • 29
Kaninchen

Klonalität

  • 54
  • 14
Monoklonal

Konjugat

  • 29
  • 5
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser SPTA1 Antikörper ist unkonjugiert

Applikation

  • 51
  • 48
  • 40
  • 9
  • 6
  • 5
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
Western Blotting (WB)
  • Verwendungszweck

    alpha 1 Spectrin Rabbit mAb

    Kreuzreaktivität

    Human, Maus, Ratte

    Produktmerkmale

    Monoclonal Antibodies

    Aufreinigung

    Affinity purification

    Immunogen

    A synthesized peptide derived from human alpha 1 Spectrin

    Isotyp

    IgG
  • Applikationshinweise

    WB,1:500 - 1:2000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    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

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    SPTA1 (Spectrin alpha 1, Erythrocytic (SPTA1))

    Andere Bezeichnung

    SPTA1

    Hintergrund

    Spectrin is an actin crosslinking and molecular scaffold protein that links the plasma membrane to the actin cytoskeleton, and functions in the determination of cell shape, arrangement of transmembrane proteins, and organization of organelles. It is a tetramer made up of alpha-beta dimers linked in a head-to-head arrangement. This gene is one member of a family of alpha-spectrin genes. The encoded protein is primarily composed of 22 spectrin repeats which are involved in dimer formation. It forms weaker tetramer interactions than non-erythrocytic alpha spectrin, which may increase the plasma membrane elasticity and deformability of red blood cells. Mutations in this gene result in a variety of hereditary red blood cell disorders, including elliptocytosis type 2, pyropoikilocytosis, and spherocytic hemolytic anemia. [provided by RefSeq, Jul 2008],EL2, HPP, HS3, SPH3, SPTA,Blood,Blood_Blood Cell Antigens,Cardiovascular,Cell Biology & Developmental Biology,Cytoskeleton,Cytoskeleton_Microfilaments,Signal Transduction,SPTA1

    Molekulargewicht

    280kDa

    Gen-ID

    6708

    UniProt

    P02549

    Pathways

    Regulation of Actin Filament Polymerization
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