CCT5 antibody (AA 210-290)
Quick Overview for CCT5 antibody (AA 210-290) (ABIN7220588)
Target
See all CCT5 AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 210-290
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Purpose
- TCP-1 ε Polyclonal Antibody
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Specificity
- TCP-1 ε Polyclonal Antibody detects endogenous levels of TCP-1 ε protein.
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Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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Immunogen
- Synthesized peptide derived from the Internal region of human TCP-1 epsilon at AA range: 210-290
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Isotype
- IgG
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Application Notes
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:10000). Not yet tested in other applications.
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Comment
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Primary Antibody
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Storage
- -20 °C
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Storage Comment
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- CCT5 (Chaperonin Containing TCP1, Subunit 5 (Epsilon) (CCT5))
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Alternative Name
- TCP-1 epsilon
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Background
- Rabbit Anti-TCP-1 ε Polyclonal Antibody,CCT5, CCTE, KIAA0098, T-complex protein 1 subunit epsilon, TCP-1-epsilon, CCT-epsilon,The chaperonin containing TCP1 subunit 5 encoded by CCT5 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.,T-complex protein 1 subunit epsilon
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Molecular Weight
- observerd band 67kDa
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Gene ID
- 22948
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UniProt
- P48643
Target
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