DC2L1 (DYNC2LI1) (NM_001012665) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC217752L4V
- LentiORF®
Lenti ORF particles, DYNC2LI1 (mGFP-tagged) - Human dynein, cytoplasmic 2, light intermediate chain 1 (DYNC2LI1), transcript variant 3, 200ul, >10^7 TU/mL
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CNY 8,550.00
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Specifications
Product Data | |
Product Name | DC2L1 (DYNC2LI1) (NM_001012665) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | CGI-60; D2LIC; DKFZp564A033; dynein, cytoplasmic 2, light intermediate chain 1; dynein 2 light intermediate chain; LIC3 |
Vector | pLenti-C-mGFP-P2A-Puro |
ACCN | NM_001012665 |
ORF Size | 1002 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC217752).
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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_001012665.1, NP_001012683.1 |
RefSeq Size | 1418 bp |
RefSeq ORF | 1004 bp |
Locus ID | 51626 |
MW | 37.3 kDa |
Gene Summary | This gene encodes a protein that is a component of the dynein-2 microtubule motor protein complex that plays a role in the retrograde transport of cargo in primary cilia via the intraflagellar transport system. This gene is ubiquitously expressed and its protein, which localizes to the axoneme and Golgi apparatus, interacts directly with the cytoplasmic dynein 2 heavy chain 1 protein to form part of the multi-protein dynein-2 complex. Mutations in this gene produce defects in the dynein-2 complex which result in several types of ciliopathy including short-rib thoracic dysplasia 15 with polydactyly (SRTD15). Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Feb 2017] |
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