| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TNPO3-DYM-20-RERE | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-REOR | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-REGO | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-REGR | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-REAQ | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-ORRE | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-OROR | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-ORGO | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-ORGR | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-ORAQ | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-GORE | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-GOOR | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-GOGO | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-GOGR | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-GOAQ | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-GRRE | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-GROR | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-GRGO | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-GRGR | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-GRAQ | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-AQRE | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-AQOR | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-AQGO | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-AQGR | 20 (40 μL) | 200 μL |
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| TNPO3-DYM-20-AQAQ | 20 (40 μL) | 200 μL |
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The protein encoded by this gene is a nuclear import receptor for serine/arginine-rich (SR) proteins such as the splicing factors SFRS1 and SFRS2. The encoded protein has also been shown to be involved in HIV-1 infection, apparently through interaction with the HIV-1 capsid protein. Two transcript variants encoding different isoforms as well as a noncoding transcript have been found for this gene.[provided by RefSeq, Jul 2010]
Gene Symbol : TNPO3
Gene Name : Transportin 3
Chromosome : CHR 7: 129,055,172-128,954,179
Locus : 7q32.1
This gene encodes a protein which regulates Golgi-associated secretory pathways that are essential to endochondral bone formation during early development. This gene is also believed to play a role in early brain development. This gene is widely expressed in embryos and is particularly abundant in chodrocytes and brain tissues. It encodes a peripheral membrane protein which shuttles between the cytosol and Golgi complex. Mutations in this gene are associated with two types of recessive osteochondrodysplasia: Dyggve-Melchior-Clausen (DMC) dysplasia and Smith-McCort (SMC) dysplasia. [provided by RefSeq, Jun 2017]
Gene Symbol : DYM
Gene Name : Dymeclin
Chromosome : CHR 18: 494,607,08-490,414,73
Locus : 18q21.1
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