| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ALG14-NRD1-20-RERE | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-REOR | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-REGO | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-REGR | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-REAQ | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-ORRE | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-OROR | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-ORGO | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-ORGR | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-ORAQ | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-GORE | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-GOOR | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-GOGO | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-GOGR | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-GOAQ | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-GRRE | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-GROR | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-GRGO | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-GRGR | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-GRAQ | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-AQRE | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-AQOR | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-AQGO | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-AQGR | 20 (40 μL) | 200 μL |
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| ALG14-NRD1-20-AQAQ | 20 (40 μL) | 200 μL |
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This gene is a member of the glycosyltransferase 1 family. The encoded protein and ALG13 are thought to be subunits of UDP-GlcNAc transferase, which catalyzes the first two committed steps in endoplasmic reticulum N-linked glycosylation. Mutations in this gene have been linked to congenital myasthenic syndrome (CMSWTA). Alternatively spliced transcript variants have been identified. [provided by RefSeq, Mar 2015]
Gene Symbol : ALG14
Gene Name : ALG14, UDP-N-acetylglucosaminyltransferase subunit
Chromosome : CHR 1: 950,729,73-949,815,64
Locus : 1p21.3
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