Mel18 (PCGF2) (NM_007144) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC202490L2V
- LentiORF®
-
Lenti ORF particles, PCGF2 (mGFP-tagged) - Human polycomb group ring finger 2 (PCGF2), 200ul, >10^7 TU/mL
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CNY 9,975.00
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Specifications
Product Data | |
Product Name | Mel18 (PCGF2) (NM_007144) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | MEL-18; RNF110; TPFS; ZNF144 |
Vector | pLenti-C-mGFP |
ACCN | NM_007144 |
ORF Size | 1032 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC202490).
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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_007144.2 |
RefSeq Size | 2622 bp |
RefSeq ORF | 1035 bp |
Locus ID | 7703 |
Domains | RING |
Protein Families | Transcription Factors |
MW | 37.8 kDa |
Gene Summary | The protein encoded by this gene contains a RING finger motif and is similar to the polycomb group (PcG) gene products. PcG gene products form complexes via protein-protein interaction and maintain the transcription repression of genes involved in embryogenesis, cell cycles, and tumorigenesis. This protein was shown to act as a negative regulator of transcription and has tumor suppressor activity. The expression of this gene was detected in various tumor cells, but is limited in neural organs in normal tissues. Knockout studies in mice suggested that this protein may negatively regulate the expression of different cytokines, chemokines, and chemokine receptors, and thus plays an important role in lymphocyte differentiation and migration, as well as in immune responses. [provided by RefSeq, Jul 2008] |
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