DIAPH1 (NM_001079812) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC213517L1V

  • LentiORF®

Lenti ORF particles, DIAPH1 (Myc-DDK tagged) - Human diaphanous homolog 1 (Drosophila) (DIAPH1), transcript variant 2, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP

Lentiviral Particles: DDK DDK w/ Puro mGFP mGFP w/ Puro


Buy this product and get 50% off on the Lenti RapidTiter kit. Use Code: Rapid50

USD 1,648.00

2 Weeks*

Size
    • 200 ul

Product Images

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Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag Myc-DDK
Symbol DIAPH1
Synonyms DFNA1; DIA1; DRF1; hDIA1; LFHL1; SCBMS
Mammalian Cell Selection None
Vector pLenti-C-Myc-DDK
ACCN NM_001079812
ORF Size 3786 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC213517).
OTI Disclaimer The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info
OTI Annotation This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene.
Reference Data
RefSeq NM_001079812.1
RefSeq Size 5777 bp
RefSeq ORF 3792 bp
Locus ID 1729
UniProt ID O60610
Cytogenetics 5q31.3
Protein Families Druggable Genome, Stem cell - Pluripotency
Protein Pathways Focal adhesion, Regulation of actin cytoskeleton
MW 140.2 kDa
Gene Summary This gene is a homolog of the Drosophila diaphanous gene, and has been linked to autosomal dominant, fully penetrant, nonsyndromic sensorineural progressive low-frequency hearing loss. Actin polymerization involves proteins known to interact with diaphanous protein in Drosophila and mouse. It has therefore been speculated that this gene may have a role in the regulation of actin polymerization in hair cells of the inner ear. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

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