| SKU | Test Kits | Buffer | Dye Color | Order Now |
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| ARHGAP29-MID2-20-RERE | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-REOR | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-REGO | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-REGR | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-REAQ | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-ORRE | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-OROR | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-ORGO | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-ORGR | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-ORAQ | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-GORE | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-GOOR | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-GOGO | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-GOGR | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-GOAQ | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-GRRE | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-GROR | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-GRGO | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-GRGR | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-GRAQ | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-AQRE | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-AQOR | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-AQGO | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-AQGR | 20 (40 μL) | 200 μL |
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| ARHGAP29-MID2-20-AQAQ | 20 (40 μL) | 200 μL |
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Rap1 is a small GTPase that, through effectors, regulates Rho GTPase signaling. These effectors- Rasip1, Radil, and the protein encoded by this gene- translocate to the cell membrane, where they form a multiprotein complex. This complex is necessary for Rap1-induced inhibition of Rho signaling. Defects in this gene may be a cause of nonsyndromic cleft lip with or without cleft palate. [provided by RefSeq, Jun 2016]
Gene Symbol : ARHGAP29
Gene Name : Rho GTPase activating protein 29
Chromosome : CHR 1: 942,750,67-941,689,06
Locus : 1p22.1
The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to microtubular structures in the cytoplasm. Alternate splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq, Feb 2009]
Gene Symbol : MID2
Gene Name : Midline 2
Chromosome : CHR X: 107,820,960-107,931,636
Locus : Xq22.3
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