MMACHC Break Apart FISH Probe
Empire Genomics’ MMACHC Break Apart FISH Probe is designed to flank the MMACHC gene and is typically used for detecting MMACHC 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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| MMACHCBA-20-ORGR (Standard Design) | 20 (40 μL) | 200 μL |
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| MMACHCBA-20-AQOR | 20 (40 μL) | 200 μL |
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| MMACHCBA-20-GOGR | 20 (40 μL) | 200 μL |
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| MMACHCBA-20-GORE | 20 (40 μL) | 200 μL |
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| MMACHCBA-20-GRGO | 20 (40 μL) | 200 μL |
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| MMACHCBA-20-GROR | 20 (40 μL) | 200 μL |
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| MMACHCBA-20-GRRE | 20 (40 μL) | 200 μL |
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| MMACHCBA-20-REGO | 20 (40 μL) | 200 μL |
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| MMACHCBA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
The exact function of the protein encoded by this gene is not known, however, its C-terminal region shows similarity to TonB, a bacterial protein involved in energy transduction for cobalamin (vitamin B12) uptake. Hence, it is postulated that this protein may have a role in the binding and intracellular trafficking of cobalamin. Mutations in this gene are associated with methylmalonic aciduria and homocystinuria type cblC. [provided by RefSeq, Oct 2009]
Gene Details
Gene Symbol: MMACHC
Gene Name: Methylmalonic Aciduria (cobalamin Deficiency) CblC Type, With Homocystinuria
Chromosome: CHR1: 45965855-45976739
Locus: 1p34.1
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: MMACHC FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: MMACHC-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping