TACD2 (TACSTD2) (NM_002353) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC202519L4V

Lenti ORF particles, TACSTD2 (mGFP-tagged) - Human tumor-associated calcium signal transducer 2 (TACSTD2), 200ul, >10^7 TU/mL

Product Images

RC202519L4 was used to prepare Lentiviral particles using TR30037 packaging kit. HEK293T cells were transduced with RC202519L4V particle to overexpress human TACSTD2-mGFP fusion protein.

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  RC202519L4 was used to prepare Lentiviral particles using TR30037 packaging kit. HEK293T cells were transduced with RC202519L4V particle to overexpress human TACSTD2-mGFP fusion protein.

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: mGFP
• Symbol: TACD2
• Synonyms: EGP-1; EGP1; GA733-1; GA7331; GP50; M1S1; TROP2
• Mammalian Cell Selection: Puromycin
• Vector: pLenti-C-mGFP-P2A-Puro
• ACCN: NM_002353
• ORF Size: 969 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC202519).
• 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_002353.1
• RefSeq Size: 2080 bp
• RefSeq ORF: 972 bp
• Locus ID: 4070
• UniProt ID: P09758
• Cytogenetics: 1p32.1
• Domains: thyroglobulin_1
• Protein Families: Druggable Genome, Transmembrane
• MW: 35.7 kDa
• Gene Summary: This intronless gene encodes a carcinoma-associated antigen. This antigen is a cell surface receptor that transduces calcium signals. Mutations of this gene have been associated with gelatinous drop-like corneal dystrophy.[provided by RefSeq, Dec 2009]