CP2c (TFCP2) (NM_005653) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC201221L1V

  • LentiORF®

Lenti ORF particles, TFCP2 (Myc-DDK tagged) - Human transcription factor CP2 (TFCP2), transcript variant 1, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP



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CNY 8,930.00


货期*
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规格
    • 200 ul

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Specifications

Product Data
Product Name CP2c (TFCP2) (NM_005653) Human Tagged ORF Clone Lentiviral Particle
Synonyms LBP1C; LSF; LSF1D; SEF; TFCP2C
Vector pLenti-C-Myc-DDK
ACCN NM_005653
ORF Size 1506 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC201221).
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_005653.3
RefSeq Size 3715 bp
RefSeq ORF 1509 bp
Locus ID 7024
Domains CP2
Protein Families Transcription Factors
MW 57.3 kDa
Gene Summary This gene encodes a transcription factor that binds the alpha-globin promoter and activates transcription of the alpha-globin gene. The encoded protein regulates erythroid gene expression, plays a role in the transcriptional switch of globin gene promoters, and it activates many other cellular and viral gene promoters. The gene product interacts with certain inflammatory response factors, and polymorphisms of this gene may be involved in the pathogenesis of Alzheimer's disease. [provided by RefSeq, Mar 2010]
*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.
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