These antibodies can be used to develop diagnostic tests for the disease.During the production of Primary Antibody, the antigens are first injected into an animal, after a period of time the serum is collected from the infected animal which will contain antibodies that specifically recognize that antigen.Now, Scientists can produce antibodies by using the immune response of animals which can be used as tools for the detection and diagnosis of diseases.Each antibody recognizes only a single antigen. On exposure to an antigen, the animal body triggers an immune response and started to produce antibodies or proteins which only recognize and bind tightly to the specific antigens.An example of a non-animal blocker is the provided NAP‐Blocker™.ĭot blot principle | Image design by Microbiologynote.Com Primary Antibodies Though, modern blocking agents apply synthetic and/or nonanimal proteins to prevent any cross-reaction with the animal antibodies.

Different blocking against is used such as dried milk powder, bovine serum albumin and casein.To prevent this, the membrane is placed in a protein mixture and the proteins block the charges that would attract the antibodies. If the membranes are not blocked then the antibodies can stick to non‐specific proteins due to their charge.This step mainly increase the specificity of the Dot blot technique by preventing non‐specific interactions. An additional crucial step is performed in dot blot techniques is known as the blocking step.Some examples of enzymes are horseradish peroxidase (HRP) and alkaline phosphatase (AP). These are catalyzed a substrate which results in the formation of either light that is recognized with radiography film, or color that is visualized on the membrane. The enzymes are the most common tags used in Dot blot technique.If a secondary antibody is applied then this will carry the tag that will help in the visualization of the protein.For example, if the primary antibody is a mouse antibody, the secondary antibody applied will identify all mouse antibodies. The secondary antibody helps to recognize the constant domain of immunoglobulin G and is species-specific.Once bound the antibody is visualized, either with a specific tag coupled to the primary antibody or with a secondary antibody.After the immobilization of proteins on a protein binding membrane (nitrocellulose or PVDF (polyvinylidene fluoride)) they are probed with a primary antibody, which is specific for the protein of interest.The main characteristic feature of dot blot is the use of immunodetection techniques for the detection of a specific protein, for example, a protein marker for a disease.To establish the importance of Dot blotting in identifying the protein of interest.Use of Dot blotting for diagnostic tests.To understand the principle of Dot Blotting.The dot blotting knew as the slot blot technique.It is considered as the most important technique in research and diagnostic laboratories used for the detection of known protein in a biological sample.This method does not offer any information on the size of the target protein.During the dot blotting, the electrophoresis of the protein samples not performed instead they are directly applied on a membrane in a single spot, and the blotting method is conducted.Dot Blot is a simplified technique of western blotting, which is mainly used for the detection of proteins.There are different blotting techniques such as Southern blotting, western blotting, and Northern blotting, etc. Dot blot is a blotting technique used for the detection of proteins.

Dot blot assay principle