| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| ARHGAP42-SBF2-20-RERE | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-REOR | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-REGO | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-REGR | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-REAQ | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-ORRE | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-OROR | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-ORGO | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-ORGR | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-ORAQ | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-GORE | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-GOOR | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-GOGO | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-GOGR | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-GOAQ | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-GRRE | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-GROR | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-GRGO | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-GRGR | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-GRAQ | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-AQRE | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-AQOR | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-AQGO | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-AQGR | 20 (40 μL) | 200 μL |
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| ARHGAP42-SBF2-20-AQAQ | 20 (40 μL) | 200 μL |
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This gene encodes a pseudophosphatase and member of the myotubularin-related protein family. This gene maps within the CMT4B2 candidate region of chromosome 11p15 and mutations in this gene have been associated with Charcot-Marie-Tooth Disease, type 4B2. [provided by RefSeq, Jul 2008]
Gene Symbol : SBF2
Gene Name : SET binding factor 2
Chromosome : CHR 11: 102,942,15-977,866,6
Locus : 11p15.4
This gene encodes a Rho GTPase-activating protein (RhoGAP), and member of the GRAF or BAR-PH family of proteins. Expression of this gene is enriched in vascular smooth muscle cells and the encoded protein inhibits RhoA activity to regulate vascular tone and control blood pressure. A mutation in the first intron of this gene modulates its expression and is associated with reduced blood pressure in human patients with borderline hypertension. [provided by RefSeq, Jul 2017]
Gene Symbol : ARHGAP42
Gene Name : Rho GTPase activating protein 42
Chromosome : CHR 11: 100,687,675-100,993,940
Locus : 11q22.1
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