MMAB Break Apart FISH Probe
Empire Genomics’ MMAB Break Apart FISH Probe is designed to flank the MMAB gene and is typically used for detecting MMAB 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 |
|---|---|---|---|---|
| MMABBA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
|
|
| MMABBA-20-AQOR | 20 (40 μL) | 200 μL |
|
|
| MMABBA-20-GOGR | 20 (40 μL) | 200 μL |
|
|
| MMABBA-20-GORE | 20 (40 μL) | 200 μL |
|
|
| MMABBA-20-GRGO | 20 (40 μL) | 200 μL |
|
|
| MMABBA-20-GRRE | 20 (40 μL) | 200 μL |
|
|
| MMABBA-20-ORGR | 20 (40 μL) | 200 μL |
|
|
| MMABBA-20-REGO | 20 (40 μL) | 200 μL |
|
|
| MMABBA-20-REGR | 20 (40 μL) | 200 μL |
|
Gene Summary
This gene encodes a protein that catalyzes the final step in the conversion of vitamin B(12) into adenosylcobalamin (AdoCbl), a vitamin B12-containing coenzyme for methylmalonyl-CoA mutase. Mutations in the gene are the cause of vitamin B12-dependent methylmalonic aciduria linked to the cblB complementation group. Alternatively spliced transcript variants have been found. [provided by RefSeq, Apr 2011]
Gene Details
Gene Symbol: MMAB
Gene Name: Methylmalonic Aciduria (cobalamin Deficiency) CblB Type
Chromosome: CHR12: 109991520-110011358
Locus: 12q24.11
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
|---|
Customer Publications
Product Details
Product: MMAB FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: MMAB-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping