PGAM2 Break Apart FISH Probe
Empire Genomics’ PGAM2 Break Apart FISH Probe is designed to flank the PGAM2 gene and is typically used for detecting PGAM2 rearrangements such as translocations. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe comes labeled in green and orange 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 |
---|---|---|---|---|
PGAM2BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL | ||
PGAM2BA-20-AQOR | 20 (40 μL) | 200 μL | ||
PGAM2BA-20-GOGR | 20 (40 μL) | 200 μL | ||
PGAM2BA-20-GORE | 20 (40 μL) | 200 μL | ||
PGAM2BA-20-GRGO | 20 (40 μL) | 200 μL | ||
PGAM2BA-20-GRRE | 20 (40 μL) | 200 μL | ||
PGAM2BA-20-ORGR | 20 (40 μL) | 200 μL | ||
PGAM2BA-20-REGO | 20 (40 μL) | 200 μL | ||
PGAM2BA-20-REGR | 20 (40 μL) | 200 μL |
Gene Summary
Phosphoglycerate mutase (PGAM) catalyzes the reversible reaction of 3-phosphoglycerate (3-PGA) to 2-phosphoglycerate (2-PGA) in the glycolytic pathway. The PGAM is a dimeric enzyme containing, in different tissues, different proportions of a slow-migrating muscle (MM) isozyme, a fast-migrating brain (BB) isozyme, and a hybrid form (MB). This gene encodes muscle-specific PGAM subunit. Mutations in this gene cause muscle phosphoglycerate mutase eficiency, also known as glycogen storage disease X. [provided by RefSeq, Sep 2009]
Gene Details
Gene Symbol: PGAM2
Gene Name: Phosphoglycerate Mutase 2
Chromosome: CHR7: 44102325-44105186
Locus: 7p13
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: PGAM2 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: PGAM2-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping