BBDS FISH Probe
The BBDS FISH probe is designed to hybridize to the BBDS 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 |
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FGFR2-20-OR (Standard Design) | 20 (40 μL) | 200 μL | ||
FGFR2-20-RE | 20 (40 μL) | 200 μL | ||
FGFR2-20-GO | 20 (40 μL) | 200 μL | ||
FGFR2-20-GR | 20 (40 μL) | 200 μL | ||
FGFR2-20-AQ | 20 (40 μL) | 200 μL | ||
FGFR2-20-DIG | 20 (40 μL) | 200 μL | ||
FGFR2-20-BIO | 20 (40 μL) | 200 μL |
Gene Summary
The protein encoded by this gene is a member of the fibroblast growth factor receptor family, where amino acid sequence is highly conserved between members and throughout evolution. FGFR family members differ from one another in their ligand affinities and tissue distribution. A full-length representative protein consists of an extracellular region, composed of three immunoglobulin-like domains, a single hydrophobic membrane-spanning segment and a cytoplasmic tyrosine kinase domain. The extracellular portion of the protein interacts with fibroblast growth factors, setting in motion a cascade of downstream signals, ultimately influencing mitogenesis and differentiation. This particular family member is a high-affinity receptor for acidic, basic and/or keratinocyte growth factor, depending on the isoform. Mutations in this gene are associated with Crouzon syndrome, Pfeiffer syndrome, Craniosynostosis, Apert syndrome, Jackson-Weiss syndrome, Beare-Stevenson cutis gyrata syndrome, Saethre-Chotzen syndrome, and syndromic craniosynostosis. Multiple alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Jan 2009]
Gene Details
Gene Symbol: FGFR2
Gene Name: Fibroblast Growth Factor Receptor 2
Chromosome: CHR10: 123237843-123357972
Locus: 10q26.13
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: BBDS FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: FGFR2-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping