NBM1 FISH Probe
The NBM1 FISH probe is designed to hybridize to the NBM1 gene and is primarily used for detecting amplifications and deletions associated with the gene. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe can be labeled in one of five colors. Each probe is sold in a 20 test kit (approximately 20 slides - 22x22 mm area) and includes hybridization buffer. Please note that due to design optimizations, prices are subject to change.
** This product is for in vitro and research use only. This product is not intended for diagnostic use.
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
NYX-20-OR (Standard Design) | 20 (40 μL) | 200 μL | ||
NYX-20-RE | 20 (40 μL) | 200 μL | ||
NYX-20-GO | 20 (40 μL) | 200 μL | ||
NYX-20-GR | 20 (40 μL) | 200 μL | ||
NYX-20-AQ | 20 (40 μL) | 200 μL | ||
NYX-20-DIG | 20 (40 μL) | 200 μL | ||
NYX-20-BIO | 20 (40 μL) | 200 μL |
Gene Summary
The product of this gene belongs to the small leucine-rich proteoglycan (SLRP) family of proteins. Defects in this gene are the cause of congenital stationary night blindness type 1 (CSNB1), also called X-linked congenital stationary night blindness (XLCSNB). CSNB1 is a rare inherited retinal disorder characterized by impaired scotopic vision, myopia, hyperopia, nystagmus and reduced visual acuity. The role of other SLRP proteins suggests that mutations in this gene disrupt developing retinal interconnections involving the ON-bipolar cells, leading to the visual losses seen in patients with complete CSNB. [provided by RefSeq, Oct 2008]
Gene Details
Gene Symbol: NYX
Gene Name: Nyctalopin
Chromosome: CHRX: 41306712-41334905
Locus: Xp11.4
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: NBM1 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: NYX-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping