EVC2 (NM_001166136) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC228654L4V
- LentiORF®
Lenti ORF particles, EVC2 (mGFP-tagged)-Human Ellis van Creveld syndrome 2 (EVC2), transcript variant 2, 200ul, >10^7 TU/mL
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CNY 22,800.00
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Specifications
Product Data | |
Product Name | EVC2 (NM_001166136) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | LBN; WAD |
Vector | pLenti-C-mGFP-P2A-Puro |
ACCN | NM_001166136 |
ORF Size | 3684 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC228654).
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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_001166136.1, NP_001159608.1 |
RefSeq Size | 4864 bp |
RefSeq ORF | 3687 bp |
Locus ID | 132884 |
Protein Families | Transmembrane |
MW | 139.9 kDa |
Gene Summary | This gene encodes a protein that functions in bone formation and skeletal development. Mutations in this gene, as well as in a neighboring gene that lies in a head-to-head configuration, cause Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia that is also known as chondroectodermal dysplasia. Mutations in this gene also cause acrofacial dysostosis Weyers type, also referred to as Curry-Hall syndrome, a disease that combines limb and facial abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009] |
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