Synaptophysin (SYP) (NM_003179) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC208972L2V

Lenti ORF particles, SYP (mGFP-tagged) - Human synaptophysin (SYP), 200ul, >10^7 TU/mL

Product Images

RC208972L2 was used to prepare Lentiviral particles using TR30037 packaging kit. HEK293T cells were transduced with RC208972L2V particle to overexpress human SYP-mGFP fusion protein.

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  RC208972L2 was used to prepare Lentiviral particles using TR30037 packaging kit. HEK293T cells were transduced with RC208972L2V particle to overexpress human SYP-mGFP fusion protein.

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: mGFP
• Symbol: Synaptophysin
• Synonyms: MRX96; MRXSYP
• Mammalian Cell Selection: None
• Vector: pLenti-C-mGFP
• ACCN: NM_003179
• ORF Size: 939 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC208972).
• 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_003179.2
• RefSeq Size: 2449 bp
• RefSeq ORF: 942 bp
• Locus ID: 6855
• UniProt ID: P08247
• Cytogenetics: Xp11.23
• Protein Families: Secreted Protein, Transmembrane
• MW: 33.9 kDa
• Gene Summary: This gene encodes an integral membrane protein of small synaptic vesicles in brain and endocrine cells. The protein also binds cholesterol and is thought to direct targeting of vesicle-associated membrane protein 2 (synaptobrevin) to intracellular compartments. Mutations in this gene are associated with an X-linked form of cognitive disability. [provided by RefSeq, Jul 2017]