THSD7A FISH Probe
Our THSD7A probe is designed to detect THSD7A amplifications and deletions. The probe comes labeled in orange, but can 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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THSD7A-20-OR (Standard Design) | 20 (40 μL) | 200 μL | ||
THSD7A-20-RE | 20 (40 μL) | 200 μL | ||
THSD7A-20-AQ | 20 (40 μL) | 200 μL | ||
THSD7A-20-GR | 20 (40 μL) | 200 μL | ||
THSD7A-20-GO | 20 (40 μL) | 200 μL |
Gene Summary
The protein encoded by this gene is found almost exclusively in endothelial cells from placenta and umbilical cord. The encoded protein appears to interact with alpha(V)beta(3) integrin and paxillin to inhibit endothelial cell migration and tube formation. This protein may be involved in cytoskeletal organization. Variations in this gene may be associated with low bone mineral density in osteoporosis. [provided by RefSeq, Aug 2010]
Gene Details
Gene Symbol: THSD7A
Gene Name: Thrombospondin Type 1 Domain Containing 7A
Chromosome: CHR7: 11410061-11871824
Locus: 7p21.3
FISH Probe Protocols
Protocol, Procedure, or Form Name | Last Modified | Download |
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