Cadherin like 23 (CDH23) (NM_052836) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC215133L4V
- LentiORF®
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Lenti ORF particles, CDH23 (mGFP-tagged) - Human cadherin-related 23 (CDH23), transcript variant 2, 200ul, >10^7 TU/mL
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Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | mGFP |
Symbol | CDH23 |
Synonyms | CDHR23; PITA5; USH1D |
Mammalian Cell Selection | Puromycin |
Vector | pLenti-C-mGFP-P2A-Puro |
ACCN | NM_052836 |
ORF Size | 1590 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC215133).
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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_052836.1, NP_443068.1 |
RefSeq Size | 2022 |
RefSeq ORF | 1593 |
Locus ID | 64072 |
Protein Families | Transmembrane |
MW | 58.4 kDa |
Gene Summary | This gene is a member of the cadherin superfamily, whose genes encode calcium dependent cell-cell adhesion glycoproteins. The encoded protein is thought to be involved in stereocilia organization and hair bundle formation. The gene is located in a region containing the human deafness loci DFNB12 and USH1D. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene. Upregulation of this gene may also be associated with breast cancer. Alternative splice variants encoding different isoforms have been described. [provided by RefSeq, May 2013] |
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