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Questions related from Israa Hassona
can anyone help me to access to uptodate site? I need to get some medical information from uptodate site but the problem is that need payment for getting password please help thank you in advanced
03 March 2018 9,671 4 View
Before ordering primer pair sequence , how can I check them? what is the accepted range of different primers properties , e.g : self complementary , haipin ......? if GC % less than 40 % for the...
10 October 2017 3,560 0 View
If the virus is positive single strand ( i.e make as mRNA ) ,I will put the genomic as an input for primer3 then click on right primer and left primer: then it gives us the forward and reverse...
10 October 2017 8,821 1 View
are The sequences of any gene in ncbi database that given in genbank file as DNA written as both strand ? or just one of them so how can we design primer F and R primer?
10 October 2017 2,583 4 View
why I have different pcr product size , although the same primer pairs sequence were used in many previous study and result the same pcr product size, but by me I have a different pcr product...
09 September 2017 5,848 8 View
I want to replace primer pair for my target gene with other primer pair for the same target but in different location , it target smaller range of sequence than the previous , so my question is...
09 September 2017 2,324 0 View
I have made extraction of brucella DNA from vagnal swab using QIAMP DNA mini kit qiagen then I made real time PCR USING applied biosystem kit for detection brucella sp. the result is strong...
09 September 2017 1,360 3 View
Hi I want to design PCR primers for Infectious Bronchitis (IB) , Can any expert tell me If the genome sequences that I will use it as input sequence for primer3 : CDS of the genome to be as cDNA ?
03 March 2017 3,885 2 View
I make DNA extraction of vaginal swab brucella then Amplification using specfic primers for Brucella meltinesis but the result was no pcr products no any band when I search I was found I MUST...
02 February 2017 6,092 3 View