Six1 Polyclonal Antibody, 20ul Cell Transfection Defects in the gene encoding

Defects in the gene encoding ARHGAP11A may cause mental retardation

Efficiently prepare for protein detection with 100 packs of TBS-T Buffer Solution

and thus suppresses apoptosis

sgRNA can be designed for different CRISPR applications

Six1 Polyclonal Antibody, 20ul Cell Transfection Defects in the gene encodingThe protein encoded by SIX1 (SIX homeobox 1)is a homeobox protein that is similar to the Drosophila 'sine oculis' gene product. SIX1 is found in a cluster of related genes on chromosome 14 and is thought to be involved in limb development. Defects in SIX1 are a cause of autosomal dominant deafness type 23 (DFNA23) and branchiootic syndrome type 3 (BOS3).