SKU: WP14714 Categories: ,

TCP-1 ε Polyclonal Antibody

Price range: $268.00 through $328.00

SKU: WP14714-100
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Product details

Background:

The protein encoded by this gene is a molecular chaperone that is a member of the chaperonin containing TCP1 complex (CCT), also known as the TCP1 ring complex (TRiC). This complex consists of two identical stacked rings, each containing eight different proteins. Unfolded polypeptides enter the central cavity of the complex and are folded in an ATP-dependent manner. The complex folds various proteins, including actin and tubulin. Mutations in this gene cause hereditary sensory and autonomic neuropathy with spastic paraplegia (HSNSP). Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 5 and 13. [provided by RefSeq, Apr 2015],

Specifications

Size50μL/100μL
TargetTCP-1 ε
ReactivityHuman, Mouse, Rat
ApplicationsWB, ELISA
MW(Calculated)
MW(Observed)67kD
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-1:2000; ELISA 1:10000; Not yet tested in other applications.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenThe antiserum was produced against synthesized peptide derived from human CCT5. AA range:241-290
SpecificityTCP-1 ε Polyclonal Antibody detects endogenous levels of TCP-1 ε protein.
Gene NameCCT5
Protein NameT-complex protein 1 subunit epsilon
Other NameCCT5; / CCTE; / KIAA0098; / T-complex protein 1 subunit epsilon; / TCP-1-epsilon; / CCT-epsilon
SpeciesHuman
Gene ID22948
UniprotP48643,
Species.1Mouse
Gene ID.112465
Uniprot.1P80316,
Species.2Rat
Gene ID.2294864
Uniprot.2Q68FQ0
Cellular LocalizationCytoplasm . Cytoplasm, cytoskeleton, microtubule organizing center, centrosome .
Tissue ExpressionBone marrow,Brain,Cajal-Retzius cell,Embryonic kidney,Fetal brain c
Signaling_pathway
Research Areas
FunctionDisease:Defects in CCT5 are the cause of autosomal recessive sensory neuropathy with spastic paraplegia [MIM:256840]. The disease is characterized by spastic paraplegia and progressive distal sensory neuropathy leading to mutilating ulcerations of the upper and lower limbs.,Function:Molecular chaperone; assist the folding of proteins upon ATP hydrolysis. Known to play a role, in vitro, in the folding of actin and tubulin.,similarity:Belongs to the TCP-1 chaperonin family.,subunit:Heterooligomeric complex of about 850 to 900 kDa that forms two stacked rings, 12 to 16 nm in diameter. Interacts with PACRG.,
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