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MHC, Class I anticorps

Cet anticorps anti-MHC, Class I est un anticorps Souris Monoclonal détectant MHC, Class I dans FACS, WB, IP, ELISA et IHC (f). Adapté pour Souris. Ce Primary Antibody a été cité dans 3+ publications.
N° du produit ABIN967374

Aperçu rapide pour MHC, Class I anticorps (ABIN967374)

Antigène

Voir toutes MHC, Class I Anticorps
MHC, Class I

Reactivité

  • 72
  • 56
  • 13
  • 10
  • 7
  • 6
  • 5
  • 5
  • 5
  • 5
  • 4
  • 1
Souris

Hôte

  • 75
  • 47
  • 7
  • 1
Souris

Clonalité

  • 91
  • 36
  • 3
Monoclonal

Conjugué

  • 36
  • 15
  • 13
  • 10
  • 3
  • 3
  • 2
  • 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
  • 1
Cet anticorp MHC, Class I est non-conjugé

Application

  • 86
  • 53
  • 33
  • 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))

Clone

SF1-1-1
  • Marque

    BD Pharmingen™

    Attributs du produit

    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.

    Purification

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

    Immunogène

    BALB/c mouse cells

    Isotype

    IgG2a kappa
  • Indications d'application

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

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Buffer

    Aqueous buffered solution containing ≤0.09 % sodium azide.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

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

    Stock

    4 °C

    Stockage commentaire

    Store undiluted at 4° C.
  • Noun, Reboul, Abastado, Jaulin, Kourilsky, Pla: "Alloreactive monoclonal antibodies select Kd molecules with different peptide profiles." dans: 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." dans: 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." dans: Journal of immunology (Baltimore, Md. : 1950), Vol. 151, Issue 7, pp. 3569-75, (1993) (PubMed).

  • Antigène

    MHC, Class I

    Autre désignation

    H-2K d

    Sujet

    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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