1. What is a TrueClone?
OriGene's TrueClones are untagged cDNA clones with native stop codons. All clones are assessed for the completeness of the open reading frame only and with respect to the associated reference. The majority of TrueClones are in the pCMV6-XL4/XL5/XL6 vectors for transient overexpression in mammalian cells. Any of our TrueClones can be provided in a vector for stable over-expression (pCMV6-Neo) for a nominal fee.
2. What is the difference between a TrueClone and a TrueORF?
TrueORFs are much more "engineered" than TrueClones. TrueORF inserts are just the coding sequence (Open Reading Frame aka ORF) in our pCMV6-Entry Precision Shuttle vector, designed to put C-terminal Myc-DDK tags on the expressed protein. TrueORFs do not contain any UTR sequences (these would interfere with making the fusion protein) but can be used for transient or stable overexpression in mammalian cells. The Open Reading Frame in any TrueORF can be easily shuttled to another destination vector adding various tags or functions.
3. Is it better to purchase a TrueClone or a TrueORF?
It really depends on the purpose of you手机500彩票客户端r experiments. For example, if you手机500彩票客户端 simply need to overexpress the protein under transient conditions, move the cDNA to you手机500彩票客户端r own vector, or use the clone as a template for PCR, then the TrueClone is a good choice. If you手机500彩票客户端 don't have a good antibody against you手机500彩票客户端r protein, need to easily purify you手机500彩票客户端r protein, or you手机500彩票客户端 need to make stable cell lines, the TrueORF is a good choice.
4. How do I search for my cDNA clone?
The most precise search of our website is by using the NCBI reference accession number of the mRNA transcript (e.g. NM_000123). This will bring up all products related to this reference sequence including TrueClone, ORF clone, antigen standard, and HuSH silencing kit. If you手机500彩票客户端 don't know the NCBI reference accession number, use the gene symbol to search. This will often generate many more hits than expected because it is a simple text search that may return many splice variants and occasionally unwanted transcripts. If you手机500彩票客户端 get too many positives, we recommend that you手机500彩票客户端 search Entrez Gene from NCBI to find the reference accession number and then repeat the search of OriGene's website with the accession number. Go to http://www.ncbi.nlm.nih.gov/ and select gene from the dropdown menu on the left of the search box.
5. How do I know the cloning sites and/or sequence of my TrueClone?
The majority of TrueClones were inserted into the pCMV6-XL4/XL5/XL6 vectors using a linker-based strategy. The linkers were ligated to the EcoRI (5`) and Sal I (3`) sites of the corresponding pCMV6-XL vector. For the 3` site, a Xho I linker was fused to the Sal I site, destroying both Xho I and Sal I in the process. These sites were not used for TrueClones in the pCMV6-AC vector (see pCMV6-AC vector map on the OriGene website). If you手机500彩票客户端 need information on the cloning sites for an AC-vector, please contact our Technical Support Team.
6. Are the cloning sites for pCMV6-AC EcoRI and Sal I?
No. Inserts were subcloned into the pCMV6-AC vector using various combinations of restriction enzymes appropriate to each specific cDNA. Please contact OriGene technical support for information on you手机500彩票客户端r specific construct.
7. Are OriGene's clones fully sequenced?
For all TrueClones, OriGene posts the available sequence data on our website in each specific clone data table (sometimes, it is necessary to access a separate ?Details and Pricing? page). 5' or 3' Read Nucleotide Sequence refers to an unedited sequence primed with a vector primer from the corresponding insert end. Sequence errors are likely to be present and therefore these reads should not be used for base-by-base analysis. Should the Open Reading Frame be covered by edited sequence, it is indicated by a link called ?Edited Nucelotide Sequence?. All TrueORF clone inserts are fully sequenced. Always note that the exact sequence of an OriGene clone may differ from the NCBI reference with respect to biological polymorphisms.
8. I received three tubes with my clone, what are they?
OriGene provides the full-length cDNA clone plus the VP1.5 (forward) and XL39 (reverse) vector sequencing primers. Should you手机500彩票客户端 need to amplify the plasmid DNA, we recommend that you手机500彩票客户端 end sequence with the VP1.5 (5') primer.
9. Can I use VP1.5 and XL39 for PCR amplication of my insert?
VP1.5, 5' GGACTTTCCAAAATGTCG 3' Tm=51C and XL39, 5' ATTAGGACAAGGCTGGTGGG 3' Tm=60C usually do not work well for amplification of the insert due to the large difference in their Tms. VP1.5 and XL39 are provided so that if you手机500彩票客户端 amplify the plasmid DNA, you手机500彩票客户端 can confirm you手机500彩票客户端r DNA prep by sequencing.
10. My VP1.5 sequence read matches the reference but my XL39 shows no BLAST similarity to anything?
Because most of OriGene's TrueClones contain a polyA tail, the XL39 primer can fail to read through this region accurately. In these instances, we recommend sequencing with a gene-specific forward primer to get a good 3` read. It is also possible that OriGene's clone has a longer UTR than was present in the reference.
11. I cannot detect any biological activity after transfecting my clone. What do I do?
Lack of activity can occur for a wide variety of causes. First, be sure that the preparation of DNA that you手机500彩票客户端 are working with is of the expected concentration and is not a purified contaminant (from you手机500彩票客户端r lab or from OriGene). Secondly, check to see if you手机500彩票客户端r protein is being expressed in you手机500彩票客户端r cell type by Western blot. If it is not, next check for expression of the mRNA transcript by RT-PCR. These are very different problems with very different solutions. Once you手机500彩票客户端 know the source of the problem, please contact our technical support scientists for assistance at 888-267-4436 (USA) or techsupport@手机500彩票客户端.
12. Is gene expression guaranteed for cDNA clones?
No. Every gene expression is different. Although the cDNA is driven by a strong promoter, mRNA can be expressed. However, a few factors can affect the steady state level of the protein of interest, including mRNA stability, protein translation efficiency and protein stability. Therefore, gene expression can not be guaranteed. This is the nature of genes. The sequence of a cDNA clone can be guaranteed to match the sequence posted on the website.
13. How can I release my insert?
In most cases, you手机500彩票客户端 can use Not I to liberate the complete insert. There are two Not I sites outside of the cloning sites in all pCMV6-XL vectors. Although it is very rare for the 8-base cutter, Not I, to cut inside a mammalian gene, it is important to verify this before employing this strategy. TrueClone inserts in pCMV6-AC can not be released using this strategy.
14. Can I use my TrueClone for in vitro transcription and translation?
Yes, we have tested our TrueClones for IVTT in rabbit reticulocyte lysate systems and have seen protein production. However, if you手机500彩票客户端r clone is in the XL4 vector, it is necessary to liberate the insert and the sense T7 promoter from the vector.
15. I need to cite you手机500彩票客户端r product for a paper I am writing. What language should I use?
We recommend that you手机500彩票客户端 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手机500彩票客户端 when you手机500彩票客户端r paper is published. Inform us and we will send a gift.