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For research use only.

Verified Samples Verified Samples in IHC: Human thyroid cancer
Dilution IHC 1:30-150
Isotype Rabbit IgG
Host Rabbit
Reactivity Human,  Mouse
Applications IHC
Clonality Polyclonal
Immunogen Fusion protein of human TRPC4AP
Abbre TRPC4AP
Synonyms C20orf188,  Chromosome 20 open reading frame 188,  member 4 associated protein,  Protein TAP1,  Protein TRUSS,  Short transient receptor potential channel 4 associated protein,  Short transient receptor potential channel 4-associated protein,  subfamily C,  TAP1 protein,  TNF receptor ubiquitous scaffol,  TNF receptor ubiquitous scaffolding/signaling protein,  TNF-receptor ubiquitous scaffolding/signaling protein,  TP4AP,  Transient receptor potential cation channel,  Trp4 associated protein,  Trp4-associated protein,  Trpc4 associated protein,  Trpc4-associated protein,  TRPC4AP,  TRRP4AP,  TRUSS,  Tumor necrosis factor receptor-associated ubiquitous scaffolding and signaling protein抗体
Swissprot
Cellular Localization Plasma Membrane, Other locations: Cul4A-RING E3 ubiquitin ligase complex.
Concentration 0.9 mg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
Purification Method Affinity purification
Research Areas Epigenetics and Nuclear Signaling,  Signal transduction
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
background TRPC4AP (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 NFκB p50, an event that occurs in response to TNF-R1 ligation. TRPC4AP exists as multiple alternatively spliced isoforms that are encoded by a gene whicHuman, Mouseaps 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.
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