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Anoctamin 3 (ANO3) (NM_031418) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC223382L1V
- LentiORF®
-
Lenti ORF particles, ANO3 (Myc-DDK tagged) - Human anoctamin 3 (ANO3), 200ul, >10^7 TU/mL
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CNY 17,290.00
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规格
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Specifications
| Product Data | |
| Product Name | Anoctamin 3 (ANO3) (NM_031418) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | C11orf25; DYT23; DYT24; GENX-3947; TMEM16C |
| Vector | pLenti-C-Myc-DDK |
| ACCN | NM_031418 |
| ORF Size | 2943 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC223382).
|
| OTI Disclaimer | Due to the inherent nature of this plasmid, standard methods to replicate additional amounts of DNA in E. coli are highly likely to result in mutations and/or rearrangements. Therefore, OriGene does not guarantee the capability to replicate this plasmid DNA. Additional amounts of DNA can be purchased from OriGene with batch-specific, full-sequence verification at a reduced cost. Please contact our customer care team at custsupport@origene.com or by calling 301.340.3188 option 3 for pricing and delivery. 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_031418.1 |
| RefSeq Size | 6641 bp |
| RefSeq ORF | 2946 bp |
| Locus ID | 63982 |
| Protein Families | Transmembrane |
| MW | 114.5 kDa |
| Gene Summary | The protein encoded by this gene belongs to the TMEM16 family of predicted membrane proteins, that are also known as anoctamins. While little is known about the function of this gene, mutations in this gene have been associated with some cases of autosomal dominant craniocervical dystonia. Cells from individuals with a mutation in this gene exhibited abnormalities in endoplasmic reticulum-dependent calcium signaling. Studies in rat show that the rat ortholog of this protein interacts with, and modulates the activity of a sodium-activated potassium channel. Deletion of this gene caused increased pain sensitivity in the rat model system. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015] |
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