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KALRN (NM_007064) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC218885L4V
- LentiORF®
-
Lenti ORF particles, KALRN (mGFP-tagged)-Human kalirin, RhoGEF kinase (KALRN), transcript variant 3, 200ul, >10^7 TU/mL
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CNY 23,750.00
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Specifications
| Product Data | |
| Product Name | KALRN (NM_007064) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | ARHGEF24; CHD5; CHDS5; DUET; DUO; HAPIP; TRAD |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_007064 |
| ORF Size | 3867 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC218885).
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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_007064.2 |
| RefSeq Size | 5729 bp |
| RefSeq ORF | 3870 bp |
| Locus ID | 8997 |
| Domains | RhoGEF, pkinase, TyrKc, PH, S_TKc, ig, IGc2, IG, FN3 |
| Protein Families | Druggable Genome, Protein Kinase |
| MW | 144.3 kDa |
| Gene Summary | Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein that interacts with the huntingtin-associated protein 1, which is a huntingtin binding protein that may function in vesicle trafficking. [provided by RefSeq, Apr 2016] |
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