AFG3L2 Break Apart FISH Probe
Empire Genomics’ AFG3L2 Break Apart FISH Probe is designed to flank the AFG3L2 gene and is typically used for detecting AFG3L2 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 |
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| AFG3L2BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| AFG3L2BA-20-AQOR | 20 (40 μL) | 200 μL |
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| AFG3L2BA-20-GOGR | 20 (40 μL) | 200 μL |
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| AFG3L2BA-20-GORE | 20 (40 μL) | 200 μL |
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| AFG3L2BA-20-GRGO | 20 (40 μL) | 200 μL |
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| AFG3L2BA-20-GRRE | 20 (40 μL) | 200 μL |
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| AFG3L2BA-20-ORGR | 20 (40 μL) | 200 μL |
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| AFG3L2BA-20-REGO | 20 (40 μL) | 200 μL |
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| AFG3L2BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders. [provided by RefSeq, Jul 2008]
Gene Details
Gene Symbol: AFG3L2
Gene Name: AFG3 Like Matrix AAA Peptidase Subunit 2
Chromosome: CHR18: 12328942-12377275
Locus: 18p11.21
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: AFG3L2 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: AFG3L2-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping