DFNB31 (WHRN) (NM_015404) Human Tagged ORF Clone

CAT#: RC220471L3

Lenti ORF clone of Human deafness, autosomal recessive 31 (DFNB31), transcript variant 1, Myc-DDK-tagged

Specifications

Product Data

• Type: Human Tagged ORF Clone
• Tag: Myc-DDK
• Symbol: WHRN
• Synonyms: CIP98; DFNB31; PDZD7B; USH2D; WI
• Vector: pLenti-C-Myc-DDK-P2A-Puro
• E. coli Selection: Chloramphenicol (34 ug/mL)
• Mammalian Cell Selection: Puromycin
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC220471).
• Restriction Sites: SgfI-MluI Cloning Scheme for this gene
• ACCN: NM_015404
• ORF Size: 2721 bp
• 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_015404.1, NP_056219.1, NP_056219.3
• RefSeq Size: 4022
• RefSeq ORF: 2724
• Locus ID: 25861
• MW: 96.4 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]