FCP1 (CTDP1) (NM_048368) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC209100L3V
- LentiORF®
Lenti ORF particles, CTDP1 (Myc-DDK-tagged)-Human CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1 (CTDP1), transcript variant 2, 200ul, >10^7 TU/mL
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CNY 8,930.00
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Specifications
Product Data | |
Product Name | FCP1 (CTDP1) (NM_048368) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | CCFDN; FCP1 |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_048368 |
ORF Size | 2601 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC209100).
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OTI Disclaimer | Due to the inherent nature of this plasmid, standard methods to replicate additional amounts of DNA in E. coli are highly likely to result in mutations and/or rearrangements. Therefore, OriGene does not guarantee the capability to replicate this plasmid DNA. Additional amounts of DNA can be purchased from OriGene with batch-specific, full-sequence verification at a reduced cost. Please contact our customer care team at custsupport@origene.com or by calling 301.340.3188 option 3 for pricing and delivery. 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_048368.3 |
RefSeq Size | 3612 bp |
RefSeq ORF | 2604 bp |
Locus ID | 9150 |
Domains | BRCT, CPDc |
Protein Families | Druggable Genome, Phosphatase, Transcription Factors |
MW | 93.3 kDa |
Gene Summary | This gene encodes a protein which interacts with the carboxy-terminus of the RAP74 subunit of transcription initiation factor TFIIF, and functions as a phosphatase that processively dephosphorylates the C-terminus of POLR2A (a subunit of RNA polymerase II), making it available for initiation of gene expression. Mutations in this gene are associated with congenital cataracts, facial dysmorphism and neuropathy syndrome (CCFDN). Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Feb 2011] |
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