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Mutations in this gene are associated with isolated steroid-17 alpha-hydroxylase deficiency
and mutations in this gene are associated with autosomal recessive spastic paraplegia-53
P110843-WB-1-P
Compatible with multi-channel pipette
Swissprot No P48431 Gene Accession NP_003097 WB Predicted band size 34 kDa WB Positive control WB Recommended dilution 500-2000 IHC predicted cell location Predicted cell location: Nucleus and Cytoplasm IHC positive control Positive control: Human gastric cancer IHC Recommed dilution Recommended dilution: 50-200 Storage
CYFIP1 rabbit monoclonal antibody Cell Culture Plates Mutations in this gene areSpecification Full name CYFIP1 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 protein that regulates cytoskeletal dynamics and protein translation. The encoded protein is a component of the WAVE regulatory complex (WRC), which promotes actin polymerization. This protein also interacts with the synaptic functional
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