PKC delta (PRKCD) (NM_006254) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC221652L2V
- LentiORF®
Lenti ORF particles, PRKCD (mGFP-tagged) - Human protein kinase C, delta (PRKCD), transcript variant 1, 200ul, >10^7 TU/mL
Lentiviral Particles: DDK DDK w/ Puro mGFP w/ Puro
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Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | mGFP |
Symbol | PKC delta |
Synonyms | ALPS3; CVID9; MAY1; nPKC-delta; PKCD |
Mammalian Cell Selection | None |
Vector | pLenti-C-mGFP |
ACCN | NM_006254 |
ORF Size | 2028 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC221652).
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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_006254.3 |
RefSeq Size | 2850 bp |
RefSeq ORF | 2031 bp |
Locus ID | 5580 |
UniProt ID | Q05655 |
Cytogenetics | 3p21.1 |
Domains | pkinase, S_TK_X, TyrKc, DAG_PE-bind, S_TKc |
Protein Families | Druggable Genome, Protein Kinase |
Protein Pathways | Chemokine signaling pathway, Fc epsilon RI signaling pathway, Fc gamma R-mediated phagocytosis, GnRH signaling pathway, Neurotrophin signaling pathway, Tight junction, Type II diabetes mellitus, Vascular smooth muscle contraction |
MW | 77.5 kDa |
Gene Summary | The protein encoded by this gene is a member of the protein kinase C family of serine- and threonine-specific protein kinases. The encoded protein is activated by diacylglycerol and is both a tumor suppressor and a positive regulator of cell cycle progression. Also, this protein can positively or negatively regulate apoptosis. Defects in this gene are a cause of autoimmune lymphoproliferative syndrome. [provided by RefSeq, Aug 2017] |
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