CCDC22 (NM_014008) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC201585L2V

  • LentiORF®

Lenti ORF particles, CCDC22 (mGFP-tagged) - Human coiled-coil domain containing 22 (CCDC22), 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP

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


Biosafety Sheet

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

USD 1,134.00

7 Weeks*

Size
    • 200 ul

Product Images

Frequently bought together (3)
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


CCDC22 mouse monoclonal antibody,clone OTI2E4
    • 100 ul

USD 447.00

Other products for "CCDC22"

Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag mGFP
Symbol CCDC22
Synonyms CXorf37; JM1; RTSC2
Mammalian Cell Selection None
Vector pLenti-C-mGFP
ACCN NM_014008
ORF Size 1881 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC201585).
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_014008.2
RefSeq Size 2333 bp
RefSeq ORF 1884 bp
Locus ID 28952
UniProt ID O60826
Cytogenetics Xp11.23
MW 70.8 kDa
Gene Summary This gene encodes a protein containing a coiled-coil domain. The encoded protein functions in the regulation of NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) by interacting with COMMD (copper metabolism Murr1 domain-containing) proteins. The mouse orthologous protein has been shown to bind copines, which are calcium-dependent, membrane-binding proteins that may function in calcium signaling. This human gene has been identified as a novel candidate gene for syndromic X-linked intellectual disability. [provided by RefSeq, Aug 2013]

{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.