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MHC, Class I Antikörper

Dieses Anti-MHC, Class I-Antikörper ist ein Maus Monoklonal-Antikörper zur Detektion von MHC, Class I in FACS, WB, IP, ELISA und IHC (f). Geeignet für Maus. Dieses Primary Antibody wurde in 3+ Publikationen zitiert.
Produktnummer ABIN967374

Kurzübersicht für MHC, Class I Antikörper (ABIN967374)

Target

Alle MHC, Class I Antikörper anzeigen
MHC, Class I

Reaktivität

  • 72
  • 45
  • 13
  • 10
  • 7
  • 6
  • 5
  • 5
  • 5
  • 5
  • 4
  • 1
Maus

Wirt

  • 65
  • 47
  • 7
  • 1
Maus

Klonalität

  • 81
  • 36
  • 3
Monoklonal

Konjugat

  • 37
  • 15
  • 12
  • 9
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser MHC, Class I Antikörper ist unkonjugiert

Applikation

  • 75
  • 54
  • 34
  • 24
  • 20
  • 15
  • 14
  • 13
  • 13
  • 11
  • 7
  • 5
  • 5
  • 3
  • 1
  • 1
  • 1
  • 1
Flow Cytometry (FACS), Western Blotting (WB), Immunoprecipitation (IP), ELISA, Immunohistochemistry (Formalin-fixed Sections) (IHC (f))

Klon

SF1-1-1
  • Marke

    BD Pharmingen™

    Produktmerkmale

    1. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
    2. Please refer to us for technical protocols.
    3. Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
    4. Sodium azide is a reversible inhibitor of oxidative metabolism, therefore, antibody preparations containing this preservative agent must not be used in cell cultures nor injected into animals. Sodium azide may be removed by washing stained cells or plate-bound antibody or dialyzing soluble antibody in sodium azide-free buffer. Since endotoxin may also affect the results of functional studies, we recommend the NA/LE™ (No Azide/Low Endotoxin) antibody format, if available, for in vitro and in vivo use.

    Aufreinigung

    The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography.

    Immunogen

    BALB/c mouse cells

    Isotyp

    IgG2a kappa
  • Applikationshinweise

    For immunohistochemical staining (IHC) of acetone-fixed frozen sections, we recommend the use of biotinylated SF1-1.1 mAb.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    0.5 mg/mL

    Buffer

    Aqueous buffered solution containing ≤0.09 % 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

    4 °C

    Informationen zur Lagerung

    Store undiluted at 4° C.
  • Noun, Reboul, Abastado, Jaulin, Kourilsky, Pla: "Alloreactive monoclonal antibodies select Kd molecules with different peptide profiles." in: Journal of immunology (Baltimore, Md. : 1950), Vol. 157, Issue 6, pp. 2455-61, (1996) (PubMed).

    Zhao, Iwata: "Cross-linking of the TCR-CD3 complex with CD4, CD8 or LFA-1 induces an anti-apoptotic signal in thymocytes: the signal is canceled by FK506." in: International immunology, Vol. 7, Issue 9, pp. 1387-96, (1996) (PubMed).

    Abastado, Casrouge, Kourilsky: "Differential role of conserved and polymorphic residues of the binding groove of MHC class I molecules in the selection of peptides." in: Journal of immunology (Baltimore, Md. : 1950), Vol. 151, Issue 7, pp. 3569-75, (1993) (PubMed).

  • Target

    MHC, Class I

    Andere Bezeichnung

    H-2K d

    Hintergrund

    The SF1-1.1 antibody reacts with the alpha3 domain of the H-2K[d] MHC class I alloantigen. Reactivity with other haplotypes (e.g, b, j, k, p, q, s, v) has not been observed. It has been reported that plate-bound SF1-1.1 mAb moderately enhances the apoptotic response of thymocytes to plate-bound 145-2C11 mAb (anti-mouse CD3e, ABIN967568 and ABIN967370). This antibody is routinely tested by flow cytometric analysis.
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