Preview

Serum Protein Electrophoresis

Satisfactory Essays
Open Document
Open Document
310 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Serum Protein Electrophoresis
Name: Fatma Al- Na'imat.
Reg. No. : 0105514.
Course: Immunology laboratory.
Instructor: Dr. Muna Hassuneh.
Report subject: Serum protein electrophoresis.
Report No.: 1.

Serum Protein Electrophoresis (SPEP)

Introduction: The serum protein electrophoresis (SPEP) test measures specific proteins in the blood to help identify some diseases. And its uses an electrical field to separate the proteins in the blood serum into groups of similar size, shape, and charge. And here we'll use gel electrophoresis which indicate that blood serum is placed on special paper treated with agarose gel and exposed to an electric current to separate the serum protein components into five major fractions by size and electrical charge: serum albumin, alpha-1 globulins, alpha-2 globulins, beta globulins, and gamma globulins. Results: As shown in next page.

Discussion: From what we observe in the gel results there are four bands and one smear, in seven lines which every line present a different serum (except 6 +7 are same 1 +2). Each band and the smear present different compound of serum protein. The first thick band is albumin which is the major fraction in a normal SPEP, and according to its concentration in serum it has the thicker band as its accounts for about 60 percent of the protein found in serum. Second band it’s a globulin protein it called Alpha-1 globulin it has the least concentration among the other globulins and albumin that’s explain the light color of its band. Third and forth bands are Alpha-2 globulin and Beta globulin respectively a close concentration values explain the bands thickness and color. The smear lastly is Gamma globulin although it has a close concentration as alpha 1 and beta globulin it has smeared zone and that’s due to its light molecular weight, so we conclude that another reason for the band thickness is the molecular weight of the

You May Also Find These Documents Helpful

  • Better Essays

    Anti-Cow Serum Lab Report

    • 1052 Words
    • 5 Pages

    Western Blot is a common used technique to identify and analyze proteins according to their ability to bind to a specific antibody. It is an analytical method that protein sample was first separate based on the molecular weight using the SDS- PAGE method, and then transferred on the nitrocellulose. The specific primary enzymes labeled antibody was used to detect the transferred protein. Antibodies bind to specific sequences of amino acids, and can recognize specific proteins among a group of many because the amino acid sequences are different from protein to protein (#3…

    • 1052 Words
    • 5 Pages
    Better Essays
  • Good Essays

    Gel electrophoresis is a technique used to separate mixtures of dna/ proteins based on what type of gel is used. Agarose gels are typically used for separating DNA and RNA. While polyacrylamide is typically used to separate out proteins and tiny amounts of nucleic acids. Gel electrophoresis of macromolecules separates molecules based on size shape length and charge. Gel electrophoresis is facilitated by the…

    • 574 Words
    • 3 Pages
    Good Essays
  • Good Essays

    The purpose of this lab is to implement the technique of gel electrophoresis in the purification and size determination of various proteins and DNA fragments. In order to do this, a polyacrylamide gel will be prepared and placed in a buffer-containing gel electrophoresis apparatus. Next, an aliquot of acid phosphatase and a molecular weight marker (Composed of Phosphorylase B, bovine serum albumin, ovalbumin, and carbonic anhydrase) will be placed into separate wells within the gel, and the apparatus will be connected to a constant voltage source (175 V) for an allotted period of time (60 min). This will allow electricity to flow through the apparatus,…

    • 1568 Words
    • 7 Pages
    Good Essays
  • Good Essays

    Western Blot Analysis

    • 476 Words
    • 2 Pages

    The western blot analyze what proteins and how much of the protein are in a gel. A western blot is very sensitive to proteins with histidine or HIS tags. Anything that contains histidine will show up in the gel. The western blot is evidence to whether or not if IL-8 is in the gel. The importances of the western blot is to show how well the proteins reacts to a disease. The first step for a western blot is to run an unstained PAGE gel. Western blot uses gel electrophoresis or electrical to arrange the proteins in order by sizes and soak up the protein into the membrane which is referred to as blotting. When blotting is done the membrane is treated with an antibody(s) to only stick to the protein that is important (IL-8 and HIS Tag). After treating…

    • 476 Words
    • 2 Pages
    Good Essays
  • Good Essays

    Allozyme analysis is a technique which is used in study of genetics because it reveals the genetic variation that exists within a wide range of organisms (Gómez, 1998). Allozymes are different forms of an enzyme expressed by alternative alleles on the same gene locus (Micales & Bonde, 1995). Analysis of these allozymes can be done by protein electrophoresis. Protein electrophoresis involves the movement of proteins within an electric field with mobility being dependent on factors such as the size and shape (secondary and tertiary structure), as well as the charge of the protein (due to primary structure). Other factors that can affect the mobility are electric-field strength, matrix pH, and ionic buffer strength of the electric field. Because there are so many factors involved in analyzing proteins during electrophoresis, it is unusual for two different proteins to have the same relative mobility (Gómez, 1998).…

    • 1385 Words
    • 4 Pages
    Good Essays
  • Good Essays

    Through the process of gel electrophoresis, DNA fragments are able to be separated. Gel electrophoresis is a method of separating and analysis DNA molecule fragments based on their size and charge. On end of the gel is given a positively charged end and one end is negatively charged. When an electric current is passed through the gel charged molecules move through it. Larger molecules move slower, moving a shorter distance, while smaller molecules move faster and traveler further. These DNA molecules are separated by size in the gel and dye is used to stain the fragments and make them more visible.…

    • 231 Words
    • 1 Page
    Good Essays
  • Good Essays

    Lab Report

    • 1398 Words
    • 6 Pages

    The homogenates provided were made by homogenizing tissues in a sucrose phosphate buffer in a 1:20 ratio. The protein concentration in bovine cells was measured by diluting the homogenate with a 1:5 ratio; 50 microliters of homogenate and 200 microliters of water. Then 5 known protein concentration samples which were 0.4, 0.8, 1.2, 1.6, 2.0 mg/ml of bovine serum were used to determine absorbance with a spectrophotometer. Two additional samples were made; one was blank and the other was for the specific homogenate sample. Then 3 microliters of bradford assay reagent, which indicates the amount of protein present by color, was added to all samples. The spectrophotometer was zeroed at 595 nm. A standard curve was made with the different absorbencies and concentrations. After the linear equation was formed, the unknown sample concentration was determined using the standard curve equation. A Gel Electrophoresis was used to perform a qualitative analysis. The use of 5 microliters of the homogenate was heated to 80 degrees Celsius. Then the homogenate was transferred to a 2-microliter-protein gel sample buffer. Samples loaded on to the gel was run at 100 v and stained with comassie blue; observations were made next lab. (Clendening 2014)…

    • 1398 Words
    • 6 Pages
    Good Essays
  • Better Essays

    Zebra Finch Lab Report

    • 1356 Words
    • 6 Pages

    The slides were prepared using the Antibody Immunohistochemistry procedure for GCR protein (PA1510A Life Technologies at 1:1000) that used DAB to stain the collected tissue to locate GCR proteins. Primary antibody is created so there is a high affinity for the protein in the experiment. For this study, the primary antibody is selective for GCR protein. The secondary antibody has a high affinity for the first, and is also bound to HRP. In the presence of GRCs, the primary antibody will bind to the GRCs.…

    • 1356 Words
    • 6 Pages
    Better Essays
  • Satisfactory Essays

    Lab 1 again

    • 768 Words
    • 3 Pages

    After completing the first portion, the secondary portion requires that one determine the protein content by measuring absorbance and various protein concentration values. There are, however, to unknown proteins with the given codes U1-K and U2-Q. By utilizing a standard curve one is able to obtain the unknown protein concentrations of BSA while also converting the absorbance readings of the unknown proteins to concentration values.…

    • 768 Words
    • 3 Pages
    Satisfactory Essays
  • Good Essays

    c) Denaturation into Single-Stranded DNA this will divide those fragments in to more distinct categories and fragment…

    • 1180 Words
    • 5 Pages
    Good Essays
  • Powerful Essays

    cell bio homework 3

    • 949 Words
    • 4 Pages

    3. You purified protein X via affinity chromatography (no diafiltration step performed) and ran an SDS-PAGE gel of the sample with a set of controls. Below is the result of your SDS-PAGE analysis.…

    • 949 Words
    • 4 Pages
    Powerful Essays
  • Good Essays

    The eggs and chicken contained lipids. These results were expected because chicken is meat, and all meats contain lipids, and the eggs contain it also because the chickens lay them.…

    • 588 Words
    • 3 Pages
    Good Essays
  • Satisfactory Essays

    Bam Bamphysics

    • 387 Words
    • 2 Pages

    Provide blood samples into separate wells. Inject a protein base into the wells. Add a primary antibody and provide a wash. Add the secondary antibody, then wash.…

    • 387 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    Nutriton lab

    • 851 Words
    • 3 Pages

    c) In a positive test for protein the colour of the substance would be pink or purple/violet…

    • 851 Words
    • 3 Pages
    Good Essays
  • Powerful Essays

    Medical Immunology

    • 2426 Words
    • 10 Pages

    • 1888, Pierre Roux & Alexander Yersin, Bacterial toxins (Yersinia pestis) • 1888, George Nuttall, Bactericidal action of blood…

    • 2426 Words
    • 10 Pages
    Powerful Essays