| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| TMEM5-PTDSS1-20-RERE | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-REOR | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-REGO | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-REGR | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-REAQ | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-ORRE | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-OROR | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-ORGO | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-ORGR | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-ORAQ | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-GORE | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-GOOR | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-GOGO | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-GOGR | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-GOAQ | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-GRRE | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-GROR | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-GRGO | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-GRGR | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-GRAQ | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-AQRE | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-AQOR | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-AQGO | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-AQGR | 20 (40 μL) | 200 μL |
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| TMEM5-PTDSS1-20-AQAQ | 20 (40 μL) | 200 μL |
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The protein encoded by this gene catalyzes the formation of phosphatidylserine from either phosphatidylcholine or phosphatidylethanolamine. Phosphatidylserine localizes to the mitochondria-associated membrane of the endoplasmic reticulum, where it serves a structural role as well as a signaling role. Defects in this gene are a cause of Lenz-Majewski hyperostotic dwarfism. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2014]
Gene Symbol : PTDSS1
Gene Name : Phosphatidylserine synthase 1
Chromosome : CHR 8: 962,618,85-963,345,51
Locus : 8q22.1
This gene encodes a type II transmembrane protein that is thought to have glycosyltransferase function. Mutations in this gene result in cobblestone lissencephaly. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2013]
Gene Symbol : TMEM5
Gene Name : Transmembrane protein 5
Chromosome : CHR 12: 637,798,02-638,095,57
Locus : 12q14.2
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