| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TRIT1-MFSD2A-20-RERE | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-REOR | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-REGO | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-REGR | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-REAQ | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-ORRE | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-OROR | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-ORGO | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-ORGR | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-ORAQ | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-GORE | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-GOOR | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-GOGO | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-GOGR | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-GOAQ | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-GRRE | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-GROR | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-GRGO | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-GRGR | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-GRAQ | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-AQRE | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-AQOR | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-AQGO | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-AQGR | 20 (40 μL) | 200 μL |
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| TRIT1-MFSD2A-20-AQAQ | 20 (40 μL) | 200 μL |
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This gene encodes a protein that that is targeted to the mitochondrion and modifies transfer RNAs (tRNAs) by adding a dimethylallyl group onto the adenine at position 37. This modification is important for maintaining the correct reading frame during protein translation. This gene is considered a tumor suppressor and its expression can decrease cell growth. Alternative splicing results in multiple transcripts variants, most of which are likely non-functional. [provided by RefSeq, Aug 2015]
Gene Symbol : TRIT1
Gene Name : TRNA isopentenyltransferase 1
Chromosome : CHR 1: 398,835,10-398,410,30
Locus : 1p34.2
The protein encoded by this gene is a transmembrane protein and sodium-dependent lysophosphatidylcholine transporter. The encoded protein is involved in the establishment of the blood-brain barrier and is required for brain growth and function. Defects in this gene are a cause of a progressive microcephaly syndrome. [provided by RefSeq, Mar 2017]
Gene Symbol : MFSD2A
Gene Name : Major facilitator superfamily domain containing 2A
Chromosome : CHR 1: 399,551,11-399,699,67
Locus : 1p34.2
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