Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

Melanoma Antigen Family A, 11 (MAGEA11) Peptide

MAGEA11 Reactivité: Mammifères Hôte: Synthetic BP, WB, IHC
N° du produit ABIN938462

Aperçu rapide pour Melanoma Antigen Family A, 11 (MAGEA11) Peptide (ABIN938462)

Antigène

MAGEA11 (Melanoma Antigen Family A, 11 (MAGEA11))

Origine

Mammifères

Source

  • 1
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • Type de proteíne

    Synthetic

    Séquence

    FSSTLNVGTL EELPAAESPS PPQSPQEESF SPTAMDAIFG SLSDEGSGSQ

    Attributs du produit

    A synthetic peptide for use as a blocking control in assays to test for specificity of MAGEA11 antibody,
    Alternative Names: MAGEA11 control peptide, MAGEA11 antibody Blocking Peptide, Anti-MAGEA11 Blocking Peptide, melanoma antigen family A, 11 Blocking Peptide, CT1.11 Blocking Peptide, MAGE-11 Blocking Peptide, MAGE11 Blocking Peptide, MAGEA-11 Blocking Peptide, MGC10511 Blocking Peptide, MAGEA11, MAGEA-11, MAGEA 11, MAGEA-11 Blocking Peptide, MAGEA 11 Blocking Peptide
  • Indications d'application

    Optimal conditions should be determined by the investigator

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.

    Buffer

    PBS

    Conseil sur la manipulation

    Avoid repeated freeze/thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20 °C long term.
  • Antigène

    MAGEA11 (Melanoma Antigen Family A, 11 (MAGEA11))

    Sujet

    This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80 % sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. Two transcript variants encoding different isoforms have been found for this gene.

    Poids moléculaire

    48 kDa
Vous êtes ici:
Chat with us!