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What color tube is done for spep?
A lavender-top tube is commonly used for performing a Serum Protein Electrophoresis (SPEP) test. This tube contains the anticoagulant EDTA.
What is the main difference between protein electrophoresis and nucleic acid electrophoresis?
There are many similarities and differences between protein and DNA electrophoresis.Similarities:PAGE protein and DNA electrophoresis both cause separation by size, creating bands that are viewed by the scientist or a machine. The smallest segments more the fastest due to less friction with the surface of their medium or equipment.The movement of charges through the medium is what causes the DNA or proteins to move. Electrons move from the negative to positive end of the gel or capillary tube.Differences:In PAGE protein electrophoresis, a polyacrylamide gel is used to prevent convection from altering the movement of the proteins. If the proteins are charged, and there is a worry that the charge will affect the mobility of the protein segments, 1% SDS can be added to get rid of the mass/charge issue. This way, only the mass of the segment determines how far it moves. In DNA capillary electrophoresis, the size of the capillary is so small that it does not have room for convection to occur (it is only 20-50 microns wide). Thus, there is no medium in the capillary but DNA itself.In protein electrophoresis, the proteins are often dyed so their movement can be viewed with the naked eye, or a machine. With DNA capillary electrophoresis, DNA strands are made through DNA replication with dNTPs that are fluorescently labeled for the different nucleotides. Each base is labeled a different color. A fine laser lights up the DNA strand in the capillary tube and reads what color fluoresces. This is how the nucleotide is identified.Protein PAGE electrophoresis is used to determine the purity of a protein sample. It can also be used to see how large the chains are that make up a multi-chain protein if a denaturing agent is added. DNA electrophoresis is used to get the order of nucleotides in a DNA sequence. It is done by chopping the DNA sequence into many smaller bits and sequencing them, then putting them back together by lining them up according to sequence overlaps. This is called the "shotgun" method. Protein electrophoresis can figure out the order of about 15-20 amino acids by a similar method, but DNA electrophoresis can get up to 1000 nucleotides (~300 amino acids). DNA electrophoresis is limited by the low probability that the DNA sequence would be cut into a segment greater than 1000 nucleotides.
What are the pros and cons of gel electrophoresis?
Pros: The detection of DNA, RNA and proteins can be done using gel electrophoresis. Gel electrophoresis does not require a large amount of starting material. Cons: difficult to extract samples for further analysis. Harmful materials.
What is done to the DNA to make the bands visible in gel electrophoresis?
In gel electrophoresis, DNA is treated with a dye that binds to the DNA molecules, making them visible as bands under ultraviolet light.
Difference between gene therapy and protein therapy?
at the gene level gene therapy is done and at the the protein level protein therapy is done
Can gel electrophoresis be used to determine the purity of an enzyme?
Gel electrophoresis can be used to assess the purity of an enzyme by separating different proteins based on size. If the enzyme appears as a single band on the gel, it suggests high purity. Contaminants or impurities would result in additional bands on the gel.
Why is destaining done after staining in agarose gel serum electrophoresis?
Destaining is done after staining in agarose gel serum electrophoresis to remove excess stain from the gel, which can interfere with visualization of the bands. Destaining helps to improve the contrast and clarity of the bands so that they can be accurately analyzed and quantified.
Can histograms be horizontal?
Conventionally, no. Which means that they can be horizontal - it is only convention stopping them. However, because you are breaking with convention, you might need to explain what you have done and why.Conventionally, no. Which means that they can be horizontal - it is only convention stopping them. However, because you are breaking with convention, you might need to explain what you have done and why.Conventionally, no. Which means that they can be horizontal - it is only convention stopping them. However, because you are breaking with convention, you might need to explain what you have done and why.Conventionally, no. Which means that they can be horizontal - it is only convention stopping them. However, because you are breaking with convention, you might need to explain what you have done and why.
Why do you use electrophoresis?
Estimation of the size of DNA molecules following restriction enzyme digestion, e.g. in restriction mapping of cloned DNA.Analysis of PCR products, e.g. in molecular genetic diagnosis or genetic fingerprintingSeparation of restricted genomic DNA prior to Southern transfer, or of RNA prior to Northern transfer.Gel electrophoresis is used in forensics, molecular biology, genetics, microbiology and biochemistry. The results can be analyzed quantitatively by visualizing the gel with UV light and a gel imaging device. The image is recorded with a computer operated camera, and the intensity of the band or spot of interest is measured and compared against standard or markers loaded on the same gel. The measurement and analysis are mostly done with specialized software.Depending on the type of analysis being performed, other techniques are often implemented in conjunction with the results of gel electrophoresis, providing a wide range of field-specific applications.
Does hemoglobin electrophoresis require fasting?
No, hemoglobin electrophoresis does not require fasting. The test can be performed at any time and is typically done using a blood sample, which does not necessitate fasting beforehand. However, it's always best to follow any specific instructions provided by your healthcare provider.
What do you use in measuring electrophoresis?
In electrophoresis, a gel or membrane is typically used for separating molecules based on their size and charge. The movement of these molecules through the gel is facilitated by an electric field. Visualizing the separated molecules is often done by staining with dyes or using specific techniques like Western blotting.
How is submarine cable constructed?
Submarine cable is constructed in much the same way direct bury cable is made. The major differences involve "what" is done rather than "how" it is done. What is done is that a whole lot of extra armor and waterproof jacketing is added. Check out the information posted by our friends at Wikipedia by using the link. The pictures alone are worth the time.
