SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
APOE-CCT5-20-RERE | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-REOR | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-REGO | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-REGR | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-REAQ | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-ORRE | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-OROR | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-ORGO | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-ORGR | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-ORAQ | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-GORE | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-GOOR | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-GOGO | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-GOGR | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-GOAQ | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-GRRE | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-GROR | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-GRGO | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-GRGR | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-GRAQ | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-AQRE | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-AQOR | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-AQGO | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-AQGR | 20 (40 μL) | 200 μL | Request Pricing | |
APOE-CCT5-20-AQAQ | 20 (40 μL) | 200 μL | Request Pricing |
The protein encoded by this gene is a major apoprotein of the chylomicron. It binds to a specific liver and peripheral cell receptor, and is essential for the normal catabolism of triglyceride-rich lipoprotein constituents. This gene maps to chromosome 19 in a cluster with the related apolipoprotein C1 and C2 genes. Mutations in this gene result in familial dysbetalipoproteinemia, or type III hyperlipoproteinemia (HLP III), in which increased plasma cholesterol and triglycerides are the consequence of impaired clearance of chylomicron and VLDL remnants. [provided by RefSeq, Jun 2016]
Gene Symbol : APOE
Gene Name : Apolipoprotein E
Chromosome : CHR 19: 449,057,48-449,093,94
Locus : 19q13.32
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]
Gene Symbol : CCT5
Gene Name : Chaperonin containing TCP1 subunit 5
Chromosome : CHR 5: 102,499,20-102,664,11
Locus : 5p15.2
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