SOX9 (NM_000346) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC208944L4V

Lenti ORF particles, SOX9 (mGFP-tagged)-Human SRY (sex determining region Y)-box 9 (SOX9), 200ul, >10^7 TU/mL

Product Images

RC208944L4 was used to prepare Lentiviral particles using TR30037 packaging kit. HEK293T cells were transduced with RC208944L4V particle to overexpress human SOX9-mGFP fusion protein.

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  RC208944L4 was used to prepare Lentiviral particles using TR30037 packaging kit. HEK293T cells were transduced with RC208944L4V particle to overexpress human SOX9-mGFP fusion protein.

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: mGFP
• Symbol: SOX9
• Synonyms: CMD1; CMPD1; SRA1; SRXX2; SRXY10
• Mammalian Cell Selection: Puromycin
• Vector: pLenti-C-mGFP-P2A-Puro
• ACCN: NM_000346
• ORF Size: 1527 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC208944).
• 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_000346.2
• RefSeq Size: 3935 bp
• RefSeq ORF: 1530 bp
• Locus ID: 6662
• UniProt ID: P48436
• Cytogenetics: 17q24.3
• Domains: HMG
• Protein Families: Adult stem cells, Druggable Genome, Embryonic stem cells, ES Cell Differentiation/IPS, Induced pluripotent stem cells, Transcription Factors
• MW: 56 kDa
• Gene Summary: The protein encoded by this gene recognizes the sequence CCTTGAG along with other members of the HMG-box class DNA-binding proteins. It acts during chondrocyte differentiation and, with steroidogenic factor 1, regulates transcription of the anti-Muellerian hormone (AMH) gene. Deficiencies lead to the skeletal malformation syndrome campomelic dysplasia, frequently with sex reversal. [provided by RefSeq, Jul 2008]