SLC22A11 Break Apart FISH Probe
Empire Genomics’ SLC22A11 Break Apart FISH Probe is designed to flank the SLC22A11 gene and is typically used for detecting SLC22A11 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 |
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SLC22A11BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
SLC22A11BA-20-AQOR | 20 (40 μL) | 200 μL | ||
SLC22A11BA-20-GOGR | 20 (40 μL) | 200 μL | ||
SLC22A11BA-20-GORE | 20 (40 μL) | 200 μL | ||
SLC22A11BA-20-GRGO | 20 (40 μL) | 200 μL | ||
SLC22A11BA-20-GROR | 20 (40 μL) | 200 μL | ||
SLC22A11BA-20-GRRE | 20 (40 μL) | 200 μL | ||
SLC22A11BA-20-REGO | 20 (40 μL) | 200 μL | ||
SLC22A11BA-20-REGR | 20 (40 μL) | 200 μL |
Gene Summary
The protein encoded by this gene is involved in the sodium-independent transport and excretion of organic anions, some of which are potentially toxic. The encoded protein is an integral membrane protein and is found mainly in the kidney and in the placenta, where it may act to prevent potentially harmful organic anions from reaching the fetus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]
Gene Details
Gene Symbol: SLC22A11
Gene Name: Solute Carrier Family 22 Member 11
Chromosome: CHR11: 64323097-64338999
Locus: 11q13.1
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: SLC22A11 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: SLC22A11-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping