DACT1 (NM_001079520) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC215557L2V

  • LentiORF®

Lenti ORF particles, DACT1 (mGFP-tagged)-Human dapper, antagonist of beta-catenin, homolog 1 (Xenopus laevis) (DACT1), 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 1,647.00

2 Weeks*

Size
    • 200 ul

Product Images

Frequently bought together (3)
DACT1 mouse monoclonal antibody,clone OTI13H4
    • 100 ul

USD 447.00


Lenti ORF control particles of pLenti-C-mGFP, >10^7 TU/mL, 0.5 mL
    • 500 ul

USD 365.00


One-Wash Lentivirus Titer Kit, HIV-1 p24 ELISA
    • 96 reactions

USD 671.00

Other products for "DACT1"

Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag mGFP
Symbol DACT1
Synonyms DAPPER; DAPPER1; DPR1; FRODO; HDPR1; TBS2; THYEX3
Mammalian Cell Selection None
Vector pLenti-C-mGFP
ACCN NM_001079520
ORF Size 2397 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC215557).
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_001079520.1
RefSeq Size 3766 bp
RefSeq ORF 2400 bp
Locus ID 51339
UniProt ID Q9NYF0
Cytogenetics 14q23.1
MW 86.2 kDa
Gene Summary The protein encoded by this gene belongs to the dapper family, characterized by the presence of PDZ-binding motif at the C-terminus. It interacts with, and positively regulates dishevelled-mediated signaling pathways during development. Depletion of this mRNA from xenopus embryos resulted in loss of notochord and head structures, and mice lacking this gene died shortly after birth from severe posterior malformations. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012]

{0} Product Review(s)

0 Product Review(s) Submit review

Be the first one to submit a review

Product Citations

*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.