Gene: GALNT17
Official Full Name: polypeptide N-acetylgalactosaminyltransferase 17provided by HGNC
Gene Summary: This gene encodes an N-acetylgalactosaminyltransferase. This gene is located centromeric to the common deleted region in Williams-Beuren syndrome (WBS), a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. This protein may play a role in membrane trafficking. [provided by RefSeq, Jan 2013]
| Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
|---|---|---|---|---|---|---|
| KOA01497 | GALNT17 Knockout cell line (293T) | Human | GALNT17 | 1:3~1:6 | negative | Online Inquiry |
| KOA07606 | GALNT17 Knockout cell line (AC16) | Human | GALNT17 | 1:3-1:4 | negative | Online Inquiry |
| KOA23051 | GALNT17 Knockout cell line (BEAS-2B) | Human | GALNT17 | 1:3~1:4 | negative | Online Inquiry |
| KOA38499 | GALNT17 Knockout cell line (U-2932) | Human | GALNT17 | 1:2-1:4 | negative | Online Inquiry |
| KOA53896 | GALNT17 Knockout cell line (TPC-1) | Human | GALNT17 | 1:5-1:8 | negative | Online Inquiry |
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