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FREM1 (NM_001177704) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC230453L3V
- LentiORF®
-
Lenti ORF particles, FREM1 (Myc-DDK-tagged)-Human FRAS1 related extracellular matrix 1 (FREM1), transcript variant 2, 200ul, >10^7 TU/mL
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CNY 13,585.00
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Specifications
| Product Data | |
| Product Name | FREM1 (NM_001177704) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | BNAR; C9orf143; C9orf145; C9orf154; MOTA; TILRR; TRIGNO2 |
| Vector | pLenti-C-Myc-DDK-P2A-Puro |
| ACCN | NM_001177704 |
| ORF Size | 2145 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC230453).
|
| 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_001177704.1 |
| RefSeq ORF | 2148 bp |
| Locus ID | 158326 |
| Protein Families | Protease, Transmembrane |
| MW | 80.7 kDa |
| Gene Summary | This gene encodes a basement membrane protein that may play a role in craniofacial and renal development. Mutations in this gene have been associated with bifid nose with or without anorectal and renal anomalies. Alternatively spliced transcript variants encoding different isoforms have been described. PubMed ID 19940113 describes one such variant that initiates transcription within a distinct, internal exon; the resulting shorter isoform (named Toll-like/interleukin-1 receptor regulator, TILRR) is suggested to be a co-receptor of the interleukin 1 receptor family and may regulate receptor function and Toll-like receptor/interleukin 1 receptor signal transduction, contributing to the control of inflammatory response activation. [provided by RefSeq, Apr 2011] |
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