The TMEM185A Polyclonal Antibody (PACO05523) is a valuable tool for researchers studying TMEM185A, a transmembrane protein known to play a role in cellular processes such as protein localization and transport. This antibody, produced in rabbits, exhibits high reactivity with human samples and has been validated for use in Western blot applications. By specifically binding to the TMEM185A protein, this antibody enables researchers to detect and analyze its expression in various cell types, making it an ideal choice for studies in cell biology and molecular biology.TMEM185A is a protein with diverse functions in cellular processes, making it a key target for research into mechanisms of protein regulation and intracellular communication.
Understanding the role of TMEM185A in cellular function has implications for a wide range of research areas, including cell signaling, protein trafficking, and disease pathology. By using the TMEM185A Polyclonal Antibody in their experiments, researchers can gain valuable insights into the biological functions of TMEM185A and its potential relevance in various physiological and pathological processes.
Synthesized peptide derived from the C-terminal region of human TMEM185A.
Form:
Liquid
Storage Buffer:
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Purification Method:
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Clonality:
Polyclonal
Isotype:
IgG
Conjugate:
Non-conjugated
Synonyms:
TMEM185A; CXorf13; FAM11A; Transmembrane protein 185A; Protein FAM11A
UniProt Protein Function:
UniProt Protein Details:
NCBI Summary:
The protein encoded by this gene is predicted to be a transmembrane protein. This gene is best known for localizing to the CpG island of the fragile site FRAXF. The 5' untranslated region of this gene contains a CGG trinucleotide repeat sequence that normally consists of 7-40 tandem CGG repeats but which can expand to greater than 300 repeats. Methylation of the CpG island leads to transcriptional silencing of this gene, but neither the silencing nor an expanded repeat region appear to manifest itself in a clear phenotypic manner. Alternative splicing results in multiple transcript variants. A pseudogene of this gene has been defined on the X chromosome. [provided by RefSeq, Aug 2013]
