
The image on the left is immunohistochemistry of paraffin-embedded Human thyroid cancer tissue using CSB-PA777153(TRPC4AP Antibody) at dilution 1/40, on the right is treated with fusion protein. (Original magnification: x200)
TRPC4AP Antibody
CSB-PA777153
ApplicationsELISA, ImmunoHistoChemistry
Product group Antibodies
TargetTRPC4AP
Overview
- SupplierCusabio
- Product NameTRPC4AP Antibody
- Delivery Days Customer20
- ApplicationsELISA, ImmunoHistoChemistry
- CertificationResearch Use Only
- ClonalityPolyclonal
- ConjugateUnconjugated
- Gene ID26133
- Target nameTRPC4AP
- Target descriptiontransient receptor potential cation channel subfamily C member 4 associated protein
- Target synonymsC20orf188; PPP1R158; protein phosphatase 1, regulatory subunit 158; short transient receptor potential channel 4-associated protein; TNF-receptor ubiquitous scaffolding/signaling protein; TRP4-associated protein; trpc4-associated protein; TRRP4AP; TRUSS; tumor necrosis factor receptor-associated ubiquitous scaffolding and signaling protein
- HostRabbit
- IsotypeIgG
- Protein IDQ8TEL6
- Protein NameShort transient receptor potential channel 4-associated protein
- Scientific DescriptionTRPC4AP (transient receptor potential cation channel, subfamily C, member 4 associated protein), also known as TRUSS or TRRP4AP, is a 797 amino acid protein that is expressed in a variety of tissues, with highest expression in liver, heart, testis and brain. Thought to function as a scaffolding protein, TRPC4AP interacts with TNF-R1 and may both link TNF-R1 to the IKK signalsome complex, and participate in the activation of NFkappaB p50, an event that occurs in response to TNF-R1 ligation. TRPC4AP exists as multiple alternatively spliced isoforms that are encoded by a gene which maps to human chromosome 20. Comprising approximately 2% of the human genome, chromosome 20 contains nearly 63 million bases that encode over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome.
- Storage Instruction-20°C or -80°C
- UNSPSC12352203