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NAIP anticorps

NAIP Reactivité: Humain ELISA, IHC Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN7239233
  • Antigène Voir toutes NAIP Anticorps
    NAIP (NLR Family, Apoptosis Inhibitory Protein (NAIP))
    Reactivité
    • 31
    • 4
    • 2
    Humain
    Hôte
    • 31
    • 1
    • 1
    Lapin
    Clonalité
    • 31
    • 2
    Polyclonal
    Conjugué
    • 16
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp NAIP est non-conjugé
    Application
    • 27
    • 13
    • 13
    • 13
    • 7
    • 5
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Attributs du produit
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogène
    Synthetic peptide of human NAIP
    Isotype
    IgG
    Top Product
    Discover our top product NAIP Anticorps primaire
  • Indications d'application
    IHC 1:25-1:100
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.5 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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
    -20 °C
    Stockage commentaire
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    NAIP (NLR Family, Apoptosis Inhibitory Protein (NAIP))
    Autre désignation
    NAIP (NAIP Produits)
    Synonymes
    anticorps BIRC1, anticorps NLRB1, anticorps psiNAIP, anticorps AV364616, anticorps Birc1a, anticorps D13Lsd1, anticorps Naip, anticorps Naip-rs1, anticorps NLR family apoptosis inhibitory protein, anticorps NLR family, apoptosis inhibitory protein 1, anticorps NAIP, anticorps Naip1
    Sujet
    This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. This copy of the gene is full length, additional copies with truncations and internal deletions are also present in this region of chromosome 5q13. It is thought that this gene is a modifier of spinal muscular atrophy caused by mutations in a neighboring gene, SMN1.
    NCBI Accession
    NP_004527
    UniProt
    Q13075
    Pathways
    Apoptose, Inflammasome
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