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NAIP Polyclonal Antibody
NAIP Polyclonal Antibody
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NAIP Polyclonal Antibody
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经销商客户: ¥214.5
实验室客户: ¥292.5
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商品描述

商品属性

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.

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