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NAIP Antikörper

NAIP Reaktivität: Human ELISA, IHC Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7239233
  • Target Alle NAIP Antikörper anzeigen
    NAIP (NLR Family, Apoptosis Inhibitory Protein (NAIP))
    Reaktivität
    • 31
    • 4
    • 2
    Human
    Wirt
    • 31
    • 1
    • 1
    Kaninchen
    Klonalität
    • 31
    • 2
    Polyklonal
    Konjugat
    • 16
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser NAIP Antikörper ist unkonjugiert
    Applikation
    • 27
    • 13
    • 13
    • 13
    • 7
    • 5
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Produktmerkmale
    Polyclonal Antibody
    Aufreinigung
    Affinity purification
    Immunogen
    Synthetic peptide of human NAIP
    Isotyp
    IgG
    Top Product
    Discover our top product NAIP Primärantikörper
  • Applikationshinweise
    IHC 1:25-1:100
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    0.5 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    NAIP (NLR Family, Apoptosis Inhibitory Protein (NAIP))
    Andere Bezeichnung
    NAIP (NAIP Produkte)
    Synonyme
    BIRC1 antikoerper, NLRB1 antikoerper, psiNAIP antikoerper, AV364616 antikoerper, Birc1a antikoerper, D13Lsd1 antikoerper, Naip antikoerper, Naip-rs1 antikoerper, NLR family apoptosis inhibitory protein antikoerper, NLR family, apoptosis inhibitory protein 1 antikoerper, NAIP antikoerper, Naip1 antikoerper
    Hintergrund
    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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