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LRRC57 anticorps

LRRC57 Reactivité: Humain, Souris, Rat ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN2423742
  • Antigène Voir toutes LRRC57 Anticorps
    LRRC57 (Leucine Rich Repeat Containing 57 (LRRC57))
    Reactivité
    • 33
    • 7
    • 5
    • 4
    • 4
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Humain, Souris, Rat
    Hôte
    • 32
    • 1
    Lapin
    Clonalité
    • 33
    Polyclonal
    Conjugué
    • 13
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp LRRC57 est non-conjugé
    Application
    • 22
    • 19
    • 14
    • 12
    • 2
    • 1
    ELISA, Immunohistochemistry (IHC)
    Purification
    Affinity purification
    Immunogène
    Recombinant protein of human LRRC57
    Isotype
    IgG
    Top Product
    Discover our top product LRRC57 Anticorps primaire
  • Indications d'application
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.2 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Agent conservateur
    Sodium azide
    Conseil sur la manipulation
    Avoid freeze / thaw cycles.
    Stock
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    LRRC57 (Leucine Rich Repeat Containing 57 (LRRC57))
    Autre désignation
    LRRC57 (LRRC57 Produits)
    Synonymes
    anticorps zgc:92240, anticorps 2810002D13Rik, anticorps AA407405, anticorps RGD1307128, anticorps leucine rich repeat containing 57, anticorps leucine rich repeat containing 57 L homeolog, anticorps lrrc57, anticorps lrrc57.L, anticorps LRRC57, anticorps Lrrc57
    Sujet
    LRRC57 (leucine rich repeat containing 57) is a 239 amino acid protein that contains eight LRR repeats and is encoded by a gene that maps to human chromosome 15q15.2. Chromosome 15 houses over 700 genes and comprises nearly 3 % of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
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