The protein encoded by this gene is a catalytic subunit of a protein complex that transfers oligosaccharides onto asparagine residues. Defects in this gene are a cause of congenital disorder of glycosylation Ix (CDG1X). [provided by RefSeq, Jun 2014]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| STT3B-20-RE | 20 (40 μL) | 200 μL |  |
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| STT3B-20-OR | 20 (40 μL) | 200 μL |  |
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| STT3B-20-GO | 20 (40 μL) | 200 μL |  |
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| STT3B-20-GR | 20 (40 μL) | 200 μL |  |
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| STT3B-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is a catalytic subunit of a protein complex that transfers oligosaccharides onto asparagine residues. Defects in this gene are a cause of congenital disorder of glycosylation Ix (CDG1X). [provided by RefSeq, Jun 2014]
Gene Symbol : STT3B
Gene Name : STT3B, catalytic subunit of the oligosaccharyltransferase complex
Chromosome : CHR 3: 315,325,00-316,376,21
Locus : 3p23
Alt. Genes : LRPPRC
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