The FAM168B Monoclonal Antibody (PAC026657) is a crucial tool for research involving FAM168B, a protein involved in various cellular processes. This antibody, produced through hybridoma technology, shows high specificity and sensitivity in detecting FAM168B in human samples. Validated for use in applications such as immunohistochemistry and Western blot, the antibody enables precise visualization and analysis of FAM168B expression in different cell types.FAM168B, also known as Family with sequence similarity 168 member B, plays a role in pathways related to cellular growth, differentiation, and metabolism. Its involvement in these processes makes it a potential target for studying diseases like cancer, metabolic disorders, and neurodegenerative conditions.
Investigating the functions of FAM168B can provide insights into the mechanisms underlying these diseases and aid in the development of targeted therapies.Overall, the FAM168B Monoclonal Antibody (PAC026657) is an essential tool for researchers interested in exploring the role of FAM168B in various biological processes and diseases. Its high specificity and reliability make it a valuable asset in advancing our understanding of cellular mechanisms and potential therapeutic targets.
Immunohistochemistry of paraffin-embedded human gastric cancer using PACO26657 at dilution of 1:100.
Immunofluorescent analysis of A549 cells using PACO26657 at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).
Immunohistochemistry of paraffin-embedded human skeletal muscle tissue using PACO26657 at dilution of 1:100.
Background:
Modulates neuronal axonal outgrowth by acting as a negative regulator of CDC42 and STAT3 and a positive regulator of STMN2. Positive regulator of CDC27.
FAM168B: Modulates neuronal axonal outgrowth by acting as a negative regulator of CDC42 and STAT3 and a positive regulator of STMN2. Positive regulator of CDC27. Belongs to the FAM168 protein family. 2 isoforms of the human protein are produced by alternative splicing.Protein type: Membrane protein, multi-passChromosomal Location of Human Ortholog: 2q21.1
