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Home TrueClone TCOF1 Clone

TCOF1 (NM_001008656) Human cDNA Clone

Specifications Citations Clones of Other Species Product Documents
SKU Description Price Availibility*  
SC301334 TCOF1 (untagged)-Human Treacher Collins-Franceschetti syndrome 1 (TCOF1), transcript variant 1 (10ug), NM_001008656.1, 10ug $2610 In Stock
TF81001 TurboFectin, High performance Transfection reagent (1ml/vial) $420 In Stock
TA311687 Rabbit polyclonal anti-TCOF1 antibody, 100ul $325 3 Weeks
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OriGene Data
Vector:pCMV6-XL5 Insert Size: 4300 Restriction Site:
Sequence Data: Fully Sequenced ORF          5' Read Nucleotide Sequence         
OTI Annotation: ORF matches with reference and there is an additional Leu at the 1135th of amino acids in ORF. This is not due to mutation because several ESTs carry the same additional amino acid.
OTI Disclaimer: Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).
Product Components: The cDNA clone is shipped in a 2-D bar-coded Matrix tube as dried plasmid DNA. The package also includes 100 pmols of both the corresponding 5' and 3' vector primers in separate vials. Every lot of primer is tested to provide clean sequencing of OriGene TrueClones.
Protein Families: Stem cell - PluripotencyDruggable Genome
Reference Data
RefSeq: NM_001008656.1, NP_001008656
RefSeq Size: 4966 RefSeq ORF: 4353
Synonyms : MFD1; treacle; treacle; Treacher Collins syndrome protein; nucleolar trafficking phosphoprotein; Treacher Collins-Franceschetti syndrome 1
LocusID: 6949 Cytogenetic: 5q32
Summary: This gene encodes a nucleolar protein with a LIS1 homology domain. The protein is involved in ribosomal DNA gene transcription through its interaction with upstream binding factor (UBF). Mutations in this gene have been associated with Treacher Collins syndrome, a disorder which includes abnormal craniofacial development. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep

Transcript Variant: This variant (1) lacks the alternate in-frame exon 21, also known as XIX, in the central coding region, compared to variant 4. The resulting isoform (a) lacks an internal segment but has the same N- and C-termini, compared to isoform d.

* Delivery time is an estimate in business days. Occasional delays may occur due to unforeseen complexities in the preparation of your construct. International customers may expect an additional 1-2 weeks in shipping

 

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