MMADHC FISH Probe
The MMADHC FISH probe is designed to hybridize to the MMADHC gene and is primarily used for detecting amplifications and deletions associated with the gene. This probe is FISH confirmed on normal peripheral blood metaphase spreads and interphase nuclei. The probe can be labeled in one of five colors. Each probe is sold in a 20 test kit (approximately 20 slides - 22x22 mm area) and includes hybridization buffer. Please note that due to design optimizations, prices are subject to change.
** 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 |
|---|---|---|---|---|
| MMADHC-20-OR (Standard Design) | 20 (40 μL) | 200 μL |  |
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| MMADHC-20-RE | 20 (40 μL) | 200 μL |  |
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| MMADHC-20-GO | 20 (40 μL) | 200 μL |  |
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| MMADHC-20-GR | 20 (40 μL) | 200 μL |  |
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| MMADHC-20-AQ | 20 (40 μL) | 200 μL |  |
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| MMADHC-20-DIG | 20 (40 μL) | 200 μL |  |
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| MMADHC-20-BIO | 20 (40 μL) | 200 μL |  |
Gene Summary
This gene encodes a mitochondrial protein that is involved in an early step of vitamin B12 metabolism. Vitamin B12 (cobalamin) is essential for normal development and survival in humans. Mutations in this gene cause methylmalonic aciduria and homocystinuria type cblD (MMADHC), a disorder of cobalamin metabolism that is characterized by decreased levels of the coenzymes adenosylcobalamin and methylcobalamin. Pseudogenes have been identified on chromosomes 11 and X.[provided by RefSeq, Nov 2008]
Gene Details
Gene Symbol: MMADHC
Gene Name: Methylmalonic Aciduria And Homocystinuria, CblD Type
Chromosome: CHR2: 150426146-150444330
Locus: 2q23.2
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: MMADHC FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: MMADHC-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping