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RFX5 anticorps (AA 237-266)

Cet anticorps Lapin Polyclonal détecte spécifiquement RFX5 dans WB. Il présente une réactivité envers Humain.
N° du produit ABIN657925

Aperçu rapide pour RFX5 anticorps (AA 237-266) (ABIN657925)

Antigène

Voir toutes RFX5 Anticorps
RFX5 (Regulatory Factor X 5 (RFX5))

Reactivité

  • 27
  • 5
  • 5
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
Humain

Hôte

  • 24
  • 3
  • 1
Lapin

Clonalité

  • 26
  • 2
Polyclonal

Conjugué

  • 24
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp RFX5 est non-conjugé

Application

  • 26
  • 16
  • 4
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB)

Clone

RB33870
  • Épitope

    • 6
    • 5
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 237-266

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogène

    This RFX5 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 237-266 amino acids from the Central region of human RFX5.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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,-20 °C

    Stockage commentaire

    RFX5 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

    Date de péremption

    6 months
  • Antigène

    RFX5 (Regulatory Factor X 5 (RFX5))

    Autre désignation

    RFX5

    Sujet

    A lack of MHC-II expression results in a severe immunodeficiency syndrome called MHC-II deficiency, or the bare lymphocyte syndrome (BLS, MIM 209920). At least 4 complementation groups have been identified in B-cell lines established from patients with BLS. The molecular defects in complementation groups B, C, and D all lead to a deficiency in RFX, a nuclear protein complex that binds to the X box of MHC-II promoters. The lack of RFX binding activity in complementation group C results from mutations in the RFX5 gene encoding the 75-kD subunit of RFX (Steimle et al., 1995). RFX5 is the fifth member of the growing family of DNA-binding proteins sharing a novel and highly characteristic DNA-binding domain called the RFX motif. Multiple alternatively spliced transcript variants have been found but the full-length natures of only two have been determined. [provided by RefSeq].

    Poids moléculaire

    65323

    ID gène

    5993

    NCBI Accession

    NP_000440, NP_001020774

    UniProt

    P48382
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