| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TMEM87B-MERTK-20-RERE | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-REOR | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-REGO | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-REGR | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-REAQ | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-ORRE | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-OROR | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-ORGO | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-ORGR | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-ORAQ | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-GORE | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-GOOR | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-GOGO | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-GOGR | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-GOAQ | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-GRRE | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-GROR | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-GRGO | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-GRGR | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-GRAQ | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-AQRE | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-AQOR | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-AQGO | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-AQGR | 20 (40 μL) | 200 μL |
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| TMEM87B-MERTK-20-AQAQ | 20 (40 μL) | 200 μL |
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This gene is a member of the MER/AXL/TYRO3 receptor kinase family and encodes a transmembrane protein with two fibronectin type-III domains, two Ig-like C2-type (immunoglobulin-like) domains, and one tyrosine kinase domain. Mutations in this gene have been associated with disruption of the retinal pigment epithelium (RPE) phagocytosis pathway and onset of autosomal recessive retinitis pigmentosa (RP). [provided by RefSeq, Jul 2008]
Gene Symbol : MERTK
Gene Name : MER proto-oncogene, tyrosine kinase
Chromosome : CHR 2: 111,898,478-112,039,945
Locus : 2q13
This gene encodes a protein that may interact with human papillomavirus type 18 E6 oncogene. The protein is also likely to be involved in endosome-to-trans-Golgi network retrograde transport. The gene is expressed in adult and fetal tissues, including brain and heart. This gene is a component of the 2q13 deletion syndrome. Mutations in this gene may be associated with congenital heart defects. [provided by RefSeq, Aug 2016]
Gene Symbol : TMEM87B
Gene Name : Transmembrane protein 87B
Chromosome : CHR 2: 112,055,222-112,119,317
Locus : 2q13
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