CLC7 (CLCN7) (NM_001114331) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC226163L3V

Lenti ORF particles, CLCN7 (Myc-DDK-tagged)-Human chloride channel 7 (CLCN7), transcript variant 2, 200ul, >10^7 TU/mL

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: Myc-DDK
• Symbol: CLCN7
• Synonyms: CLC-7; CLC7; HOD; OPTA2; OPTB4; PPP1R63
• Mammalian Cell Selection: Puromycin
• Vector: pLenti-C-Myc-DDK-P2A-Puro
• ACCN: NM_001114331
• ORF Size: 2343 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC226163).
• 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_001114331.2, NP_001107803.1
• RefSeq Size: 4164 bp
• RefSeq ORF: 2346 bp
• Locus ID: 1186
• UniProt ID: P51798
• Cytogenetics: 16p13.3
• Protein Families: Druggable Genome, Ion Channels: Other, Transmembrane
• MW: 86 kDa
• Gene Summary: The product of this gene belongs to the CLC chloride channel family of proteins. Chloride channels play important roles in the plasma membrane and in intracellular organelles. This gene encodes chloride channel 7. Defects in this gene are the cause of osteopetrosis autosomal recessive type 4 (OPTB4), also called infantile malignant osteopetrosis type 2 as well as the cause of autosomal dominant osteopetrosis type 2 (OPTA2), also called autosomal dominant Albers-Schonberg disease or marble disease autosoml dominant. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. OPTA2 is the most common form of osteopetrosis, occurring in adolescence or adulthood. [provided by RefSeq, Jul 2008]