Kdm2b (NM_001003953) Mouse Tagged ORF Clone Lentiviral Particle
CAT#: MR211909L3V
- LentiORF®
Lenti ORF particles, Kdm2b (Myc-DDK-tagged) - Mouse lysine (K)-specific demethylase 2B (Kdm2b), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 18,715.00
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Specifications
Product Data | |
Product Name | Kdm2b (NM_001003953) Mouse Tagged ORF Clone Lentiviral Particle |
Synonyms | Cxxc2; Fbl10; Fbxl1; Fbxl10; Jhdm1b; PCCX2 |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_001003953 |
ORF Size | 3927 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(MR211909).
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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_001003953.1 |
RefSeq Size | 5184 bp |
RefSeq ORF | 3930 bp |
Locus ID | 30841 |
Gene Summary | The protein encoded by this gene is a H3K36-specific histone demethylase, which contains an N-terminal jumonji C domain, a CxxC zinc finger domain, a plant homeodomain finger, an F-box, and eight leucine-rich repeats. Amongst its demonstrated functions, this protein plays roles in the suppression of premature cellular senescence, leukemia maintenance and development, maintenance of mouse embryonic stem cell pluripotency, and induced pluripotent stem cell generation. Mice homozygous for a targeted deletion of the zinc finger domain display embryonic lethality with development ceasing at approximately 7 to 8 days post coitum, demonstrating an essential role in early development. A pseudogene of this gene is found on chromosome 4. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014] |
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