NAIP Polyclonal Antibody

    • Catalog No.:YT6052
    • Applications:IHC;IF;ELISA
    • Reactivity:Human;Mouse
      • Target:
      • NAIP
      • Fields:
      • >>NOD-like receptor signaling pathway;>>Pathogenic Escherichia coli infection;>>Shigellosis;>>Salmonella infection;>>Legionellosis
      • Gene Name:
      • NAIP BIRC1
      • Protein Name:
      • Baculoviral IAP repeat-containing protein 1 (Neuronal apoptosis inhibitory protein)
      • Human Gene Id:
      • 4671
      • Human Swiss Prot No:
      • Q13075
      • Immunogen:
      • Synthetic peptide from human protein at AA range: 1191-1240
      • Specificity:
      • The antibody detects endogenous NAIP
      • Formulation:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • Source:
      • Polyclonal, Rabbit,IgG
      • Dilution:
      • IHC 1:50-200, ELISA 1:10000-20000. IF 1:50-200
      • Purification:
      • The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
      • Concentration:
      • 1 mg/ml
      • Storage Stability:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • Other Name:
      • Baculoviral IAP repeat-containing protein 1 (Neuronal apoptosis inhibitory protein)
      • Background:
      • 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. The protein encoded by this gene contains regions of homology to two baculovirus inhibitor of apoptosis proteins, and it is able to suppress apoptosis induced by various signals. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by Ref
      • Function:
      • disease:Mutated or deleted forms of NAIP have been found in individuals with severe spinal muscular atrophy (SMA) leading to the hypothesis that mutations in the NAIP locus may contribute to the SMA phenotype.,function:Prevents motor-neuron apoptosis induced by a variety of signals.,similarity:Contains 1 NACHT domain.,similarity:Contains 3 BIR repeats.,tissue specificity:Expressed in motor neurons, but not in sensory neurons. Found in liver and placenta, and to a lesser extent in spinal cord.,
      • Subcellular Location:
      • cytoplasm,basolateral plasma membrane,neuron projection,perikaryon,extracellular exosome,
      • Expression:
      • Expressed in motor neurons, but not in sensory neurons. Found in liver and placenta, and to a lesser extent in spinal cord.
      • Products Images
      • Immunohistochemical analysis of paraffin-embedded Human-placenta, antibody was diluted at 1:100