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TrueORF Clones and PrecisionShuttle System

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What is the PrecisionShuttle System?
What is the difference between OriGene抯 Entry vector and the destination vectors?
What are the functional aspects of the pCMV6-AC-GFP vector?
OriGene抯 GFP is listed as TurboGFP. How is this different from other available GFPs?
Has OriGene fully sequenced all TrueORF clones?
Do TrueORF clones exactly match the reference gene sequence?
Sequences of the sequencing primers, VP1.5, XL39, pTUNE-F Forward and pTUNE-R Reverse
Can I transfer large ORFs using this system?
What restriction enzymes should I use if Sgf I or Mlu I sites are present in my ORF?
Why does my Certificate of Authorization (COA) indicate cloning sites other than Sgf I and Mlu I?
What sites should I use to transfer a TrueORF clone into the Gateway system?
What restriction sites are available for subcloning into other vectors?
How many amino acids are present in the linker between my protein and tGFP?
Which vector serves the negative control for the GFP fusion clone?
Can I purchase the empty Entry vector without any open reading frame?
I don抰 see any expression. What should I do?
What does your disclaimer mean?
What is the TrueORF Guarantee?
I need to cite your product for a paper I am writing. What language should I use?
How can I improve the efficiency of my SgfI digestion?

Q: What is the PrecisionShuttle System?
A: The PrecisionShuttle System provides a restriction-enzyme-based ap琾roach to append different tags to one抯 open reading frame (ORF) of interest.

Q: What is the difference between OriGene抯 Entry vector and the destination vectors?
A: The major differences are the antibiotic selection marker and the epitope tags. The Entry vector carries kanamycin resistance (25 ug/ml), while all destina瑃ion vectors contain the ampicillin resistance gene (100 ug/ml). This allows simple screening for successful subcloning products. All of the vectors have a unique combination of N- and C-terminal epitope tags or a fluorescent marker, as de瑂cribed in Table I.

Q: What are the functional aspects of the pCMV6-AC-GFP vector?
A: Like all OriGene vectors, the CMV promoter drives the heterologous expression of the specified open reading frame (ORF) which is in-frame with Turbo Green Fluorescent Protein (tGFP) on the C-terminus. tGFP expression permits the positive identification of mammalian cells transfected with plasmid. The neomycin resistance gene is also expressed downstream of the SV40 promoter within the same vector and permits positive selection of transfected cells as well as stable cell line production. For bacterial amplification, the ampicillin resistance gene is engineered on the opposite strand.

Q: OriGene抯 GFP is listed as TurboGFP. How is this different from other available GFPs?
A: TurboGFP is a fully licensed, 26kDA protein product from Evrogen JSC 17 that works well in standardized GFP assays. Excitation max is 482nm and emis瑂ion max is 502nm. It yields 112% of the brightness compared to eGFP and has no known cellular toxicity. It is an isoform of the naturally occurring protein from Pontellina plumata that has been optimized for rapid labeling of cells/organelles and tracking of promoter activity. It is a perfect choice for monitoring transient protein expression.

Q: Has OriGene fully sequenced all TrueORF clones?
A: Not always. When transferring the cDNA into the TrueORF Entry Vector, OriGene always uses fully sequenced plasmids as templates and Phusion High-Fi琩elity DNA Polymerase (New England Biolabs), which has a mutation rate less than 4 x 10-7. This ensures the highest fidelity of every TrueORF clone. After cloning into the Entry vector, each of OriGene抯 TrueORF clones was sequenced at both the 5?and 3?ends, and the resulting sequence was matched to the corresponding reference sequence. For ORFs of 1 Kb or less in length, the 5?and 3?sequencing reads have covered the full ORF. For longer cDNAs, the ORF was not fully covered by sequencing reads.

Q: Do TrueORF clones exactly match the reference gene sequence?
A: All TrueORF clones are guaranteed to match the corresponding ORF sequence posted on our website. However, some clones may contain nucleotide changes compared to the published reference sequences. This is due to SNPs (single nucleotide polymorphisms) reflecting the unique differences from genes expressed in different tissues and different individuals. Published references may represent a different SNP than the OriGene transcript. Should a specific SNP be required, this can be obtained via our Gene Synthesis service.

Q: Sequences of the sequencing primers, VP1.5, XL39, pTUNE-F Forward and pTUNE-R Reverse
A: VP1.5 (forward seq primer)
5?GGACTTTCCAAAATGTCG 3?Tm=51C
XL39 (reverse seq primer)
5?ATTAGGACAAGGCTGGTGGG 3?Tm=60C
pTUNE-F Forward
5?TAGAGTCGACCTGCAGCCGG 3?Tm=58C
pTUNE-R Reverse
5?TCGCTGATTTGTGTAGGGGA 3?Tm=52C

Q: Can I transfer large ORFs using this system?
A: It has been reported that ORFs larger than 4 Kb are unstable in recombi琻ation-based systems; conversely, our restriction digest-based vector system has no real size limitation. An ORF up to 18 Kb can be readily transferred from one vector to another.

Q: What restriction enzymes should I use if Sgf I or Mlu I sites are present in my ORF?
A: While 96% of all human and mouse ORFs can use the Sgf I - Mlu I com琤ination, some ORFs do contain internal Mlu I site(s). Most of those ORFs with an internal Mlu I site can be transferred using another rare cutter (Rsr II), whose re瑂triction site is upstream of Mlu I, or Not I, whose site is immediately downstream of Mlu I. Using one of the four different subcloning combinations, any ORF can be transferred from one vector to another. The recommended subcloning combina瑃ion for every TrueORF cDNA is listed in the product information on our website.

Q: Why does my Certificate of Authorization (COA) indicate cloning sites other than Sgf I and Mlu I?
A: Whenever one or both of these sites is present within the ORF of the tran瑂cript, the PrecisionShuttle vectors share other sites engineered to accommodate this, e.g. Rsr II or Asc I.

Q: What sites should I use to transfer a TrueORF clone into the Gateway system?
A: There are multiple sites in pCMV6-Entry than can be used to move the insert of a TrueORF clone into one of Gateway抯 Entry vectors (pENTR-1A, -2B, -3C, -4, and -11). These sites are EcoRI, Sal I, BamHI and Kpn I at the 5?end, and Not I at the 3?end.

Q: What restriction sites are available for subcloning into other vectors?
A: The vector map and nucleotide sequence can be found at http://www.origene.com/cdna/trueorf/destinationvector.aspx

Q: How many amino acids are present in the linker between my protein and tGFP?
A: To accommodate the Mlu I cloning site, which maintains the proper read琲ng frame, this vector appends a threonine and arginine. This is far fewer than with other recombination-based shuttling systems.

Q: Which vector serves the negative control for the GFP fusion clone?
A: We recommend pCMV6-AN-GFP (Cat# PS100019).

Q: Can I purchase the empty Entry vector without any open reading frame?
A: Yes, The catalog number is PS100010 for a lyophilized 10 ug aliquot. Alternatively, you can release the ORF from the Entry vector with Xho I and Sal I, and then religate to create the empty Entry vector control.

Q: I don抰 see any expression. What should I do?
A: First, check your transfection efficiency. We recommend using a plasmid that expresses a fluorescent marker for this purpose, e.g. our pCMV-AN-GFP des瑃ination vector, PS100019. If the transfection efficiency is over 80% and there is no detectable expression from the ORF, please contact OriGene抯 technical support group at 301-340-3188 or 888-267-4436 for Ph.D. level assistance. If no solution is obvious, they will work with you to run the appropriate control experiments. Sometimes, this means that new test constructs or replacement constructs will be offered free of charge. OriGene is invested in your success and excellent post-sales support is available.

Q: What does your disclaimer mean?
A: OriGene抯 disclaimer for the TrueORF clones reads as follows: 揙ur mo琹ecular clone sequence data has been matched to the accession number below as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding accession number, e.g., by representing an alternative RNA splicing form or single nucleotide polymor-phism (SNP).? The NCBI RefSeq mRNA sequences are continuously being revised, as some may have been derived from aberrantly spliced transcripts or generated by incorrect prediction of intron-exon junctions in silico. These sequences are therefore used only as a 搑eference?and not as a 搒tandard? OriGene抯 clones are isolated from full-length cDNA libraries and may differ from the reference sequence for this reason.

Q: What is the TrueORF Guarantee?
A: OriGene warrants that the product will meet specifications listed. At OriGene抯 discretion, free replacement of any non-conforming product will be made if OriGene is notified within 30 days of product receipt. If you experience any difficulty with any OriGene product, please contact our Technical Support Staff at 888-267-4436, or 301-340-3188 outside the US.

Q: I need to cite your product for a paper I am writing. What language should I use?
A: We recommend that you refer to the product by its specific catalog number and refer to us as OriGene Technologies (Rockville, MD). Furthermore, we'd love to hear from you when your paper is published. Inform us and we will send a gift.

Q: How can I improve the efficiency of my SgfI digestion?
A: We have heard that there can be lot-to-lot variations of the commercially available SgfI enzyme. Several of our scientists have begun to use the "FastDigest?AsiSI (SfaAI) " enzyme (Fermentas) that has the same recognition sequence. In our hands the double digestions with MluI are complete in a shorter time using this enzyme compared to some but not all SgfI batches.

 

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