FOXI1 (NM_144769) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC206430L3V

  • LentiORF®

Lenti ORF particles, FOXI1 (Myc-DDK tagged) - Human forkhead box I1 (FOXI1), transcript variant 2, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP



Need custom lentivirus service?
Get a free quote

CNY 8,170.00


货期*
详询

规格
    • 200 ul

Product images

经常一起买 (3)
Lenti ORF control particles of pLenti-C-Myc-DDK-P2A-Puro, >1x10^7 TU/ml, 0.5 ml
    • 500 ul

CNY 2,950.00


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

CNY 5,230.00


FOXI1 mouse monoclonal antibody, clone OTI2G6 (formerly 2G6)
    • 100 ul

CNY 1,999.00
CNY 2,700.00

Specifications

Product Data
Product Name FOXI1 (NM_144769) Human Tagged ORF Clone Lentiviral Particle
Synonyms FKH10; FKHL10; FREAC-6; FREAC6; HFH-3; HFH3
Vector pLenti-C-Myc-DDK-P2A-Puro
ACCN NM_144769
ORF Size 849 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC206430).
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_144769.2, NP_658982.1
RefSeq Size 2011 bp
RefSeq ORF 852 bp
Locus ID 2299
Protein Families Transcription Factors
MW 30.8 kDa
Gene Summary This gene belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain. This gene may play an important role in the development of the cochlea and vestibulum, as well as in embryogenesis. The encoded protein has been found to be required for the transcription of four subunits of a proton pump found in the inner ear, the kidney, and the epididymis. Mutations in this gene have been associated with deafness, autosomal recessive 4. [provided by RefSeq, Jan 2017]
*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.
Customer Reviews 
Loading...