The C1orf112 Polyclonal Antibody (PAC041818) is a vital tool for researchers studying C1orf112, a protein involved in a variety of cellular processes. This antibody, generated in rabbits, is highly specific for human samples and has been validated for use in techniques such as Western blotting. By targeting the C1orf112 protein, this antibody allows for precise detection and analysis in different cell types, making it ideal for investigations in areas such as cell biology and disease research.
C1orf112, also known as a potential regulatory protein, plays a crucial role in the regulation of various cellular functions, making it a promising target for studying diseases like cancer, neurodegenerative disorders, and metabolic diseases. Understanding the function of C1orf112 is essential for uncovering its potential role in disease development and progression, as well as for developing targeted therapies that can manipulate its activity for therapeutic purposes.
Antibody Name:
C1orf112 Antibody (PACO41418)
Antibody SKU:
PACO41418
Size:
50ug
Host Species:
Rabbit
Tested Applications:
ELISA, IHC
Recommended Dilutions:
ELISA:1:2000-1:10000, IHC:1:20-1:200
Species Reactivity:
Human
Immunogen:
Recombinant Human Uncharacterized protein C1orf112 protein (301-530AA)
Immunohistochemistry of paraffin-embedded human thyroid tissue using PACO41418 at dilution of 1:100.
Immunohistochemistry of paraffin-embedded human cervical cancer using PACO41418 at dilution of 1:100.
Synonyms:
Uncharacterized protein C1orf112, C1orf112
UniProt Protein Function:
UniProt Protein Details:
NCBI Summary:
This gene represents a member of the formin family of proteins. It is considered a diaphanous formin due to the presence of a diaphanous inhibitory domain located at the N-terminus of the encoded protein. Studies of a similar mouse protein indicate that the protein encoded by this locus may function in polymerization and depolymerization of actin filaments. Mutations at this locus have been associated with focal segmental glomerulosclerosis 5.[provided by RefSeq, Aug 2010]
