SKU | Test Kits | Buffer | Dye Color | Order Now |
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TGFBR2-XPC-20-RERE | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-REOR | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-REGO | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-REGR | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-REAQ | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-ORRE | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-OROR | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-ORGO | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-ORGR | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-ORAQ | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-GORE | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-GOOR | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-GOGO | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-GOGR | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-GOAQ | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-GRRE | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-GROR | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-GRGO | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-GRGR | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-GRAQ | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-AQRE | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-AQOR | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-AQGO | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-AQGR | 20 (40 μL) | 200 μL |
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TGFBR2-XPC-20-AQAQ | 20 (40 μL) | 200 μL |
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The protein encoded by this gene is a transmembrane protein that has a protein kinase domain, forms a heterodimeric complex with TGF-beta receptor type-1, and binds TGF-beta. This receptor/ligand complex phosphorylates proteins, which then enter the nucleus and regulate the transcription of genes related to cell proliferation, cell cycle arrest, wound healing, immunosuppression, and tumorigenesis. Mutations in this gene have been associated with Marfan Syndrome, Loeys-Deitz Aortic Aneurysm Syndrome, and the development of various types of tumors. Alternatively spliced transcript variants encoding different isoforms have been characterized. [provided by RefSeq, Aug 2017]
Gene Symbol : TGFBR2
Gene Name : Transforming growth factor beta receptor 2
Chromosome : CHR 3: 306,064,89-306,941,41
Locus : 3p24.1
The protein encoded by this gene is a key component of the XPC complex, which plays an important role in the early steps of global genome nucleotide excision repair (NER). The encoded protein is important for damage sensing and DNA binding, and shows a preference for single-stranded DNA. Mutations in this gene or some other NER components can result in Xeroderma pigmentosum, a rare autosomal recessive disorder characterized by increased sensitivity to sunlight with the development of carcinomas at an early age. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2017]
Gene Symbol : XPC
Gene Name : XPC complex subunit, DNA damage recognition and repair factor
Chromosome : CHR 3: 141,786,71-141,451,46
Locus : 3p25.1
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