FMRP (FMR1) (NM_002024) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC222699L1V

  • LentiORF®

Lenti ORF particles, FMR1 (Myc-DDK tagged) - Human fragile X mental retardation 1 (FMR1), transcript variant ISO1, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP

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


Special Offer: Buy this product and get 50% off Lenti Control Particles. Learn More.

USD 1,432.00

2 Weeks*

Size
    • 200 ul

Product Images

Frequently bought together (3)
Lenti ORF control particles of pLenti-C-Myc-DDK, >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


FMR1 (FMRP ) mouse monoclonal antibody, clone OTI1C6 (formerly 1C6)
    • 100 ul

USD 447.00

Other products for "FMRP"

Specifications

Product Data
Type Human Tagged ORF Clone Lentiviral Particle
Tag Myc-DDK
Symbol FMRP
Synonyms FMRP; FRAXA; POF; POF1; POFX
Mammalian Cell Selection None
Vector pLenti-C-Myc-DDK
ACCN NM_002024
ORF Size 1896 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC222699).
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_002024.3
RefSeq Size 4362 bp
RefSeq ORF 1899 bp
Locus ID 2332
UniProt ID Q06787
Cytogenetics Xq27.3
Domains KH
Protein Families Druggable Genome
MW 71 kDa
Gene Summary The protein encoded by this gene binds RNA and is associated with polysomes. The encoded protein may be involved in mRNA trafficking from the nucleus to the cytoplasm. A trinucleotide repeat (CGG) in the 5' UTR is normally found at 6-53 copies, but an expansion to 55-230 repeats is the cause of fragile X syndrome. Expansion of the trinucleotide repeat may also cause one form of premature ovarian failure (POF1). Multiple alternatively spliced transcript variants that encode different protein isoforms and which are located in different cellular locations have been described for this gene. [provided by RefSeq, May 2010]

{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.