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What else can I help you with?
How do you predict a PCR product size from a gene cloned into an expression vector?
It all depends on where you primers are. Presumably you will have one primer that sits on the cloned gene and one that sits on the vector (that way you only get a product if the gene has cloned successfully). As long as you know where your primers land, it should be easy to work out how big the PCR product will be simply by adding the distance from the primer on the gene to the end of the gene and the distance from the primer on the vector to the end of the vector.
How do you extend concrete setting time?
you can buy primers from you local hardware or diy store to extend setting time
What end of a growing strand are DNA nucleotides added to?
5' end (nucleotides are added from 3' toward 5')
If you were to stretch all the DNA in all our cells end to end from the earth to the sun how many rounds can we go?
we can go about 5 times from the earth to to sun
How are telomeres important for preserving eukaryotic genes?
Telomeres solve the end replication problem by extending the 3' end of the chromosome. Without them, the 3' end can't be replicated since replication is 5' to 3'.
What are the release dates for Everyday Food - 2004 Pasta Primers 5-7?
Everyday Food - 2004 Pasta Primers 5-7 was released on: USA: 21 February 2009
Can aspartic acid be phosphorylated in biological systems?
Yes, aspartic acid can be phosphorylated in biological systems.
Which amino acids can be phosphorylated in biological systems?
In biological systems, amino acids such as serine, threonine, and tyrosine can be phosphorylated.
Which protein can be phosphorylated by protein kinase AA?
The protein that can be phosphorylated by protein kinase AA is called protein X.
Can aspartate be phosphorylated in biological systems?
Yes, aspartate can be phosphorylated in biological systems through the addition of a phosphate group to its structure.
Why are two different primers required for the polymerase chain reaction?
Must use the forward and reverse primers to bind to complementary sequence at the 3' end of the template strand - each NEW strand is built in 5' to 3' direction. They flank the targeted gene region - must attach one to each strand of the target DNA.
Does PCR use RNA primers in its process?
No, PCR (polymerase chain reaction) uses DNA primers, not RNA primers, in its process.
Differences between primary and secondary active transport?
In primary active transport, the transport protein gets phosphorylated; in secondary active transport, the transport protein is not phosphorylated
How can one create primers for PCR effectively?
To create primers for PCR effectively, start by selecting a target DNA sequence and designing primers that are specific to that sequence. Ensure the primers have similar melting temperatures and avoid self-complementarity. Test the primers for efficiency and specificity using PCR before proceeding with the experiment.
What are the benefits of using the TaqMan Gene Expression Assays?
TaqMan Gene Expression Assays consist of a pair of unlabeled PCR primers and a TaqMan probe with a FAM or VIC dye label on the 5' end, and minor groove binder (MGB) nonfluorescent quencher (NFQ) on the 3' end.
What happens once glucose is phosphorylated?
Becomes trapped in the cell
How many primers are typically used in Sanger sequencing?
In Sanger sequencing, typically two primers are used.
