DOK7 (NM_001164673) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC228191L3V
- LentiORF®
Lenti ORF particles, DOK7 (Myc-DDK-tagged)-Human docking protein 7 (DOK7), transcript variant 2, 200ul, >10^7 TU/mL
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Specifications
Product Data | |
Product Name | DOK7 (NM_001164673) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | C4orf25; CMS1B; CMS10; FADS3 |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_001164673 |
ORF Size | 765 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC228191).
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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_001164673.1 |
RefSeq ORF | 768 bp |
Locus ID | 285489 |
MW | 27.3 kDa |
Gene Summary | The protein encoded by this gene is essential for neuromuscular synaptogenesis. The protein functions in aneural activation of muscle-specific receptor kinase, which is required for postsynaptic differentiation, and in the subsequent clustering of the acetylcholine receptor in myotubes. This protein can also induce autophosphorylation of muscle-specific receptor kinase. Mutations in this gene are a cause of familial limb-girdle myasthenia autosomal recessive, which is also known as congenital myasthenic syndrome type 1B. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009] |
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