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Mutations associated with this gene cause autosomal recessive spastic paraplegia 13
May suppress cell migration and invasion activity
Full name STK39 rabbit monoclonal antibody Alternative names 50 μl/100 μl Reactivity rabbit monoclonal Applications WB
Overexpression of this gene may play a role in both cancer and diabetes
TIAM2 rabbit monoclonal antibody package:50 μl Mutations associated with this geneSpecification Full name TIAM2 rabbit monoclonal antibody Alternative names 50 l 100 l Reactivity rabbit monoclonal Applications WB Host Rabbit Clone type rabbit monoclonal Target Background This gene encodes a guanine nucleotide exchange factor. A highly similar mouse protein specifically activates ras related C3 botulinum substrate 1, converting this Rho like guanosine triphosphatase (GTPase) from a guanosine diphosphate bound inactive state to a
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