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R&D Systems™ Human Nyctalopin/NYX (NP_072089) VersaClone cDNA
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:
10 μg
Description
- Also known as: CLRP; NBM1; CSNB1; CSNB4; CSNB1A
- NYX belongs to the small leucinerich proteoglycan (SLRP) family of proteins.
- Defects in NYX are the cause of congenital stationary night blindness type 1 (CSNB1), also called X-linked congenital stationary night blindness (XLCSNB).
- The role of other SLRP proteins suggests that mutations in NYX disrupt developing retinal interconnections involving the ON-bipolar cells, leading to the visual losses seen in patients with complete CSNB.
- The insert is sequence verified and the entire plasmid DNA and insert translated sequences are provided.
- For reasearch use only. Not for use in humans.
Specifications
Specifications
| Gene | hNYX |
| Accession Number | NP_072089 |
| Concentration | 10 μg at 0.2 μg/μL |
| Formulation | cDNA is provided in 10 mM Tris-Cl, pH 8.5 |
| Insert Type | 1459 bp |
| Gene ID (Entrez) | 60506 |
| Content And Storage | Store the unopened product at -20°C to -70°C. Use a manual defrost freezer and avoid repeated freeze-thaw cycles. Do not use past expiration date. |
| Species | Human |
| Quantity | 10 μg |
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