TNFAIP8L2-SCNM1 Break Apart FISH Probe
Empire Genomics’ TNFAIP8L2-SCNM1 Break Apart FISH Probe is designed to flank the TNFAIP8L2-SCNM1 gene and is typically used for detecting TNFAIP8L2-SCNM1 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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TNFAIP8L2-SCNM1BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL | ||
TNFAIP8L2-SCNM1BA-20-AQOR | 20 (40 μL) | 200 μL | ||
TNFAIP8L2-SCNM1BA-20-GOGR | 20 (40 μL) | 200 μL | ||
TNFAIP8L2-SCNM1BA-20-GORE | 20 (40 μL) | 200 μL | ||
TNFAIP8L2-SCNM1BA-20-GRGO | 20 (40 μL) | 200 μL | ||
TNFAIP8L2-SCNM1BA-20-GROR | 20 (40 μL) | 200 μL | ||
TNFAIP8L2-SCNM1BA-20-GRRE | 20 (40 μL) | 200 μL | ||
TNFAIP8L2-SCNM1BA-20-REGO | 20 (40 μL) | 200 μL | ||
TNFAIP8L2-SCNM1BA-20-REGR | 20 (40 μL) | 200 μL |
Gene Summary
This locus represents naturally occurring read-through transcription between the neighboring TNFAIP8L2 (tumor necrosis factor, alpha-induced protein 8-like 2) and SCNM1 (sodium channel modifier 1) genes on chromosome 1. The protein-coding read-through transcript variant encodes a protein that shares sequence identity with the downstream gene product but its N-terminal region is shorter due to alternate exon use relative to the downstream gene. [provided by RefSeq, Dec 2016]
Gene Details
Gene Symbol: TNFAIP8L2-SCNM1
Gene Name: TNFAIP8L2-SCNM1 Readthrough
Chromosome: CHR1: 151129104-151142773
Locus: 1q21.3
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: TNFAIP8L2-SCNM1 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: TNFAIP8L2-SCNM1-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping