| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TF-CCT5-20-RERE | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-REOR | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-REGO | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-REGR | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-REAQ | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-ORRE | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-OROR | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-ORGO | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-ORGR | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-ORAQ | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-GORE | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-GOOR | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-GOGO | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-GOGR | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-GOAQ | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-GRRE | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-GROR | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-GRGO | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-GRGR | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-GRAQ | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-AQRE | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-AQOR | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-AQGO | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-AQGR | 20 (40 μL) | 200 μL |
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| TF-CCT5-20-AQAQ | 20 (40 μL) | 200 μL |
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This gene encodes a glycoprotein with an approximate molecular weight of 76.5 kDa. It is thought to have been created as a result of an ancient gene duplication event that led to generation of homologous C and N-terminal domains each of which binds one ion of ferric iron. The function of this protein is to transport iron from the intestine, reticuloendothelial system, and liver parenchymal cells to all proliferating cells in the body. This protein may also have a physiologic role as granulocyte/pollen-binding protein (GPBP) involved in the removal of certain organic matter and allergens from serum. [provided by RefSeq, Sep 2009]
Gene Symbol : TF
Gene Name : Transferrin
Chromosome : CHR 3: 133,661,997-133,779,005
Locus : 3q22.1
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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