FGD1 Break Apart FISH Probe
Empire Genomics’ FGD1 Break Apart FISH Probe is designed to flank the FGD1 gene and is typically used for detecting FGD1 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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| FGD1BA-20-GROR (Standard Design) | 20 (40 μL) | 200 μL |
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| FGD1BA-20-AQOR | 20 (40 μL) | 200 μL |
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| FGD1BA-20-GOGR | 20 (40 μL) | 200 μL |
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| FGD1BA-20-GORE | 20 (40 μL) | 200 μL |
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| FGD1BA-20-GRGO | 20 (40 μL) | 200 μL |
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| FGD1BA-20-GRRE | 20 (40 μL) | 200 μL |
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| FGD1BA-20-ORGR | 20 (40 μL) | 200 μL |
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| FGD1BA-20-REGO | 20 (40 μL) | 200 μL |
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| FGD1BA-20-REGR | 20 (40 μL) | 200 μL |
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Gene Summary
This gene encodes a protein that contains Dbl (DH) and pleckstrin (PH) homology domains and is similar to the Rho family of small GTP-binding proteins. The encoded protein specifically binds to the Rho family GTPase Cdc42Hs and can stimulate the GDP-GTP exchange of the isoprenylated form of Cdc42Hs. It also stimulates the mitogen activated protein kinase cascade leading to c-Jun kinase SAPK/JNK1 activation. Defects in this gene are the cause of the faciogenital dysplasia in Aarskog-Scott syndrome and a syndromatic form of X-linked cognitive disability. [provided by RefSeq, Jul 2017]
Gene Details
Gene Symbol: FGD1
Gene Name: FYVE, RhoGEF And PH Domain Containing 1
Chromosome: CHRX: 54471886-54522599
Locus: Xp11.22
FISH Probe Protocols
| Protocol, Procedure, or Form Name | Last Modified | Download |
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Customer Publications
Product Details
Product: FGD1 FISH Probe
Test Kits: 20 (40 μL)
ISH Buffer: 200 μL
SKU: FGD1-20-OR
Material Safety Data Sheet: MSDS.pdf
Turnaround Time: 7-10 Business Days
Shipping Time: 1-2 Day Expedited Shipping