CCDC22 Break Apart FISH Probe
Empire Genomics’ CCDC22 Break Apart FISH Probe is designed to flank the CCDC22 gene and is typically used for detecting CCDC22 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in orange and green by default, but may be customized to meet your needs.
** 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 |
---|---|---|---|---|
CCDC22BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
CCDC22BA-20-AQOR | 20 (40 μL) | 200 μL | ||
CCDC22BA-20-GOGR | 20 (40 μL) | 200 μL | ||
CCDC22BA-20-GORE | 20 (40 μL) | 200 μL | ||
CCDC22BA-20-GRGO | 20 (40 μL) | 200 μL | ||
CCDC22BA-20-GROR | 20 (40 μL) | 200 μL | ||
CCDC22BA-20-GRRE | 20 (40 μL) | 200 μL | ||
CCDC22BA-20-REGO | 20 (40 μL) | 200 μL | ||
CCDC22BA-20-REGR | 20 (40 μL) | 200 μL |
Gene Summary
This gene encodes a protein containing a coiled-coil domain. The encoded protein functions in the regulation of NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) by interacting with COMMD (copper metabolism Murr1 domain-containing) proteins. The mouse orthologous protein has been shown to bind copines, which are calcium-dependent, membrane-binding proteins that may function in calcium signaling. This human gene has been identified as a novel candidate gene for syndromic X-linked intellectual disability. [provided by RefSeq, Aug 2013]
Gene Details
Gene Symbol: CCDC22
Gene Name: Coiled-coil Domain Containing 22
Chromosome: CHRX: 49091926-49106987
Locus: Xp11.23
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: CCDC22 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: CCDC22-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping