TFDP1 Polyclonal Antibody, 100ul Dialysis Defects in PAK3 are the

Defects in PAK3 are the cause of non-syndromic mental retardation X-linked type 30 (MRX30)

Mutations in this gene cause cystinosis| a lysosomal storage disorder

These enzymes play a critical role in collagen chain assembly

ERF2/ZDHHC9 subfamily

TFDP1 Polyclonal Antibody, 100ul Dialysis Defects in PAK3 are theTFDP1 encodes a member of a family of transcription factors that heterodimerize with E2F proteins to enhance their DNA binding activity and promote transcription from E2F target genes. The encoded protein functions as part of this complex to control the transcriptional activity of numerous genes involved in cell cycle progression from G1 to S phase. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene are found on