MMRN1 Break Apart FISH Probe
Empire Genomics’ MMRN1 Break Apart FISH Probe is designed to flank the MMRN1 gene and is typically used for detecting MMRN1 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 |
|---|---|---|---|---|
| MMRN1BA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| MMRN1BA-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| MMRN1BA-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| MMRN1BA-20-GORE | 20 (40 μL) | 200 μL |
|
|
| MMRN1BA-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| MMRN1BA-20-GROR | 20 (40 μL) | 200 μL |
|
|
| MMRN1BA-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| MMRN1BA-20-REGO | 20 (40 μL) | 200 μL |
|
|
| MMRN1BA-20-REGR | 20 (40 μL) | 200 μL |
|
Gene Summary
Multimerin is a massive, soluble protein found in platelets and in the endothelium of blood vessels. It is comprised of subunits linked by interchain disulfide bonds to form large, variably sized homomultimers. Multimerin is a factor V/Va-binding protein and may function as a carrier protein for platelet factor V. It may also have functions as an extracellular matrix or adhesive protein. Recently, patients with an unusual autosomal-dominant bleeding disorder (factor V Quebec) were found to have a deficiency of platelet multimerin. [provided by RefSeq, Jul 2008]
Gene Details
Gene Symbol: MMRN1
Gene Name: Multimerin 1
Chromosome: CHR4: 90816051-90875780
Locus: 4q22.1
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|
Customer Publications
Product Details
Product: MMRN1 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: MMRN1-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping