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PCDH11X (NM_032968) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC222228L4V
- LentiORF®
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Lenti ORF particles, PCDH11X (mGFP-tagged) - Human protocadherin 11 X-linked (PCDH11X), transcript variant c, 200ul, >10^7 TU/mL
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CNY 24,035.00
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Specifications
| Product Data | |
| Product Name | PCDH11X (NM_032968) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | PCDH-X; PCDH-Y; PCDH11; PCDH11Y; PCDH22; PCDHX; PPP1R119 |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_032968 |
| ORF Size | 4041 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC222228).
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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_032968.2 |
| RefSeq Size | 9176 bp |
| RefSeq ORF | 4044 bp |
| Locus ID | 27328 |
| Domains | CA |
| Protein Families | Transmembrane |
| MW | 145.1 kDa |
| Gene Summary | This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. The encoded protein consists of an extracellular domain containing 7 cadherin repeats, a transmembrane domain and a cytoplasmic tail that differs from those of the classical cadherins. The gene is located in a major X/Y block of homology and its Y homolog, despite divergence leading to coding region changes, is the most closely related cadherin family member. The protein is thought to play a fundamental role in cell-cell recognition essential for the segmental development and function of the central nervous system. Disruption of this gene may be associated with developmental dyslexia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014] |
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