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DIAPH3


Official Full Name
diaphanous related formin 3
Organism
Homo sapiens
Gene ID
81624
Background
This gene encodes a member of the diaphanous subfamily of the formin family. Members of this family are involved in actin remodeling and regulate cell movement and adhesion. Mutations in this gene are associated with autosomal dominant auditory neuropathy 1. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]
Synonyms
AN; DIA2; DRF3; AUNA1; NSDAN; diap3; mDia2

Cat.No. Product Name Price
SHH005321 shRNA set against Human DIAPH3(NM_001042517.1) Inquiry
SHH005339 shRNA set against Human DIAPH3(NM_030932.3) Inquiry
SHH278045 shRNA set against Human DIAPH3 (NM_030932.3) Inquiry
SHW006935 shRNA set against Danio rerio DIAPH3 (NM_001003624) Inquiry
Cat.No. Product Name Price
CDFH005074 Human DIAPH3 cDNA Clone(NM_001042517.1) Inquiry
MiUTR1H-02823 DIAPH3 miRNA 3'UTR clone Inquiry
MiUTR1H-02824 DIAPH3 miRNA 3'UTR clone Inquiry
CDCB168410 Danio rerio DIAPH3 ORF Clone (NM_001003624) Inquiry
CDCB190863 Rabbit DIAPH3 ORF clone (XM_008260036.1) Inquiry
CDCR055550 Human DIAPH3 ORF clone (NM_001042517.1) Inquiry
CDCR310864 Human DIAPH3 ORF Clone(NM_030932.3) Inquiry
CDCS407112 Human DIAPH3 ORF Clone (BC048963) Inquiry
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