| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TSEN2-PPARG-20-RERE | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-REOR | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-REGO | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-REGR | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-REAQ | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-ORRE | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-OROR | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-ORGO | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-ORGR | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-ORAQ | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-GORE | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-GOOR | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-GOGO | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-GOGR | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-GOAQ | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-GRRE | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-GROR | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-GRGO | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-GRGR | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-GRAQ | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-AQRE | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-AQOR | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-AQGO | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-AQGR | 20 (40 μL) | 200 μL |
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| TSEN2-PPARG-20-AQAQ | 20 (40 μL) | 200 μL |
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This gene encodes a member of the peroxisome proliferator-activated receptor (PPAR) subfamily of nuclear receptors. PPARs form heterodimers with retinoid X receptors (RXRs) and these heterodimers regulate transcription of various genes. Three subtypes of PPARs are known: PPAR-alpha, PPAR-delta, and PPAR-gamma. The protein encoded by this gene is PPAR-gamma and is a regulator of adipocyte differentiation. Additionally, PPAR-gamma has been implicated in the pathology of numerous diseases including obesity, diabetes, atherosclerosis and cancer. Alternatively spliced transcript variants that encode different isoforms have been described. [provided by RefSeq, Jul 2008]
Gene Symbol : PPARG
Gene Name : Peroxisome proliferator activated receptor gamma
Chromosome : CHR 3: 122,878,49-124,710,53
Locus : 3p25.2
This gene encodes one of the subunits of the tRNA splicing endonuclease. This endonuclease catalyzes the first step in RNA splicing which is the removal of introns. Mutations in this gene have been associated with pontocerebellar hypoplasia type 2. A pseudogene has been identified on chromosome 4. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Feb 2009]
Gene Symbol : TSEN2
Gene Name : TRNA splicing endonuclease subunit 2
Chromosome : CHR 3: 124,844,31-125,396,23
Locus : 3p25.2
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