This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
Facts about All-trans-retinol dehydrogenase [NAD(+)] ADH4.
Human | |
---|---|
Gene Name: | ADH4 |
Uniprot: | P08319 |
Entrez: | 127 |
Belongs to: |
---|
zinc-containing alcohol dehydrogenase family |
ADH-2; alcohol dehydrogenase 4 (class II), pi polypeptide; alcohol dehydrogenase 4; Alcohol dehydrogenase class II pi chain; aldehyde reductase; EC 1.1.1; EC 1.1.1.1
Mass (kDA):
40.222 kDA
Human | |
---|---|
Location: | 4q23 |
Sequence: | 4; NC_000004.12 (99123657..99144298, complement) |
Cytoplasm.
In addition to providing high-affinity primary antibodies for the ADH4 marker, Boster also offers gene infographics and reagents with a variety of other high-quality features. These antibodies are consistently cited in scientific journals and have been validated for use in Western Blotting, Immunohistochemistry, and ELISA. Here are some examples of these tools:
Monoclonal antibodies are the most popular types of primary antibodies for research. They are produced by raising antibodies against a single epitope, resulting in high specificity and low non-specific cross-reactivity. While traditional mouse monoclonal antibodies have been used for various research applications, new techniques are now allowing scientists to raise antibodies against other species. Boster Bio High-affinity primary antibodies using the ADH4 marker is the most recent monoclonal antibody from the company.
Developed by Boster Bio, this product utilizes an innovative, dual-labeling method. This unique method enables researchers to ask more questions of specimens with a single antibody, while simultaneously identifying the target antigen. This allows researchers to obtain richer answers and more contextual data. This unique combination is ideal for researchers looking to monitor the spread of cancer. These high-affinity antibodies are made from human monoclonal antigens and have an 80% affinity to cancer cells.
Boster Bio High-affinity primary antibodies are highly specific and have exceptional binding affinity for human IgM. This antibody reacts with human and mouse samples in WB and IHC, and is supplied as a 100ul Liquid. It has been cited in a variety of scientific papers and has maintained its popularity for over 25 years. With a broad range of applications, it is sure to be the right choice for your next research project.
The ADH4 marker has been proven to be extremely useful in antibody testing. The ADH4 marker was specifically designed for the specificity of this antibody. This antibody binds to a single epitope on the target protein. This method is widely used for assessing the specificity of monoclonal antibodies. The ADH4 marker has a high affinity and specificity score, making it a perfect choice for researchers with sensitive diagnostics.
The ER stress response is a known sequela to obesity-induced renal damage. The ADH4 marker, GRP78, and CHOP were found to be more highly expressed in obese mice than in nonobese controls. FXR activation attenuated the ER-induced apoptosis in obese mice and ameliorated its effects. Similarly, FXR-activated mice exhibited reduced expression of caspase-3. These findings suggest that FXR activation can protect proximal tubular cells from ER stress.
RNA was isolated from the right kidney of a healthy adult mouse using SDS-PAGE. The protein was then blotted onto a polyvinylidene difluoride membrane. The membrane was blocked with 0.1% Tween 20 and incubated with antibodies overnight. Horseradish peroxidase was used to conjugate antibodies and the staining was detected using an ECL Plus detection system. Antibodies used for the staining were anti-Villin antibody (Chemicon) and anti-Osta antibody (Santa Cruz Biotechnology).
Histological staining methods have undergone major changes throughout the history of histology. Modern histology incorporates both chemical staining and molecular biology techniques. Early histologists used readily available chemicals such as alcohol, mercuric chloride, carmine, silver nitrate, and Giemsa stains. These stains are often accompanied by other techniques such as immunohistochemistry.
Nuclear Fast Red, an optimized nuclear counterstain solution, provides intense nuclear staining. This anionic dye, used in conjunction with aluminium salt as a mordant, allows for fast staining, with a single step. Nuclear Fast Red stains the nucleus in less than five minutes. Its rapid staining ability makes it a good alternative to hematoxylin, and is useful in multiple labeling and for direct application to tissue sections.
One of the most important features of a Boster Bio antibody is its high affinity. Their antibodies are highly specific and characterized by high affinity. Additionally, they are validated for IHC, WB, FC, and ELISA. These antibodies are available in rabbit polyclonal and mouse monoclonal varieties. You can also get a free secondary antibody when purchasing any of their products. If you need additional antibodies, Boster Bio has thousands of high affinity, low-cost antibodies that will meet your needs.
Molecular Pathology Core Laboratory (MPCL) is dedicated to advancing molecular pathology-based cancer research. The team works as a central hub for collaborative research and facilitates genetic discovery in primary human tumors. The laboratory also provides services for image analysis, reporting, and design assistance. Whether you need a slide stained for IHC or an IHC assay, Boster Bio provides a comprehensive histology service that will help you reach your clinical goals.
The Boster Bio guide offers a step-by-step protocol for immunohistochemistry (IHC). The guide includes detailed illustrations and recommended reagents. The guide also covers sample preparation techniques, including antigen retrieval, fixation, embedding, and sample optimization. In addition to a guide for different types of preserved tissues, the Boster Bio website also provides detailed information on how to prepare samples for IHC. For a high-quality stain, you must follow the proper protocol for your tissues.
PMID: 3036213 by Hoeoeg J.-O., et al. Structure of the class II enzyme of human liver alcohol dehydrogenase: combined cDNA and protein sequence determination of the pi subunit.
PMID: 1889753 by von Bahr-Lindstroem H., et al. Cloning and characterization of the human ADH4 gene.