DFNB31 (WHRN) (NM_001083885) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC213282L3V
- LentiORF®
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Lenti ORF particles, DFNB31 (Myc-DDK-tagged)-Human deafness, autosomal recessive 31 (DFNB31), transcript variant 2, 200ul, >10^7 TU/mL
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CNY 8,930.00
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Specifications
Product Data | |
Product Name | DFNB31 (WHRN) (NM_001083885) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | CIP98; DFNB31; PDZD7B; USH2D; WI |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_001083885 |
ORF Size | 1572 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC213282).
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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_001083885.2, NP_001077354.2 |
RefSeq Size | 2915 bp |
RefSeq ORF | 1575 bp |
Locus ID | 25861 |
MW | 55.6 kDa |
Gene Summary | This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016] |
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