The Anti-EDA Chimeric Recombinant Rabbit Monoclonal Antibody (HDAB0256) is a powerful research tool for studying EDA, a cell surface protein involved in cell adhesion and signaling processes. This antibody, generated using cutting-edge recombinant technology, offers high specificity and sensitivity for detecting EDA in various biological samples.With its unique chimeric structure, the HDAB0256 antibody combines the benefits of both rabbit monoclonal antibodies and recombinant antibodies, resulting in superior performance in applications such as immunohistochemistry, flow cytometry, and ELISA. Its ability to specifically target EDA makes it an invaluable asset for researchers investigating the role of this protein in processes like development, wound healing, and cancer progression.
By using the HDAB0256 antibody, scientists can gain deeper insights into the function of EDA and its potential implications in various physiological and pathological conditions. Its versatility and reliability make it a must-have tool for studies in cell biology, molecular biology, and biochemistry. Unlock the mysteries of EDA with the Anti-EDA Chimeric Recombinant Rabbit Monoclonal Antibody (HDAB0256) and enhance your research capabilities today.
SKU:
HDAB0256
Size:
100 µg
Clonality:
Monoclonal
Clone:
DMC388
Synonyms:
ED1; EDA2
Applications:
Flow Cyt
Recommended Dilution:
Flow Cyt 1:100
Host Species:
Rabbit
Isotype:
Rabbit/Human Fc chimeric IgG1
Reactivity:
Human
Purification Method:
Purified from cell culture supernatant by affinity chromatography
Formulation:
Powder
Buffer:
1XPBS
Storage:
Store at -20°C to -80°C for 12 months in lyophilized form. After reconstitution, if not intended for use within a month, aliquot and store at -80°C (Avoid repeated freezing and thawing).Lyophilized antibodies are shipped at ambient temperature.
Usage:
Research use only
Background:
The protein encoded by this gene is a type II membrane protein that can be cleaved by furin to produce a secreted form. The encoded protein, which belongs to the tumor necrosis factor family, acts as a homotrimer and may be involved in cell-cell signaling during the development of ectodermal organs. Defects in this gene are a cause of ectodermal dysplasia, anhidrotic, which is also known as X-linked hypohidrotic ectodermal dysplasia. Several transcript variants encoding many different isoforms have been found for this gene.
