The LHFPL6 Monoclonal Antibody (PAC027949) is a cutting-edge tool for investigating LHFPL6, a transmembrane protein involved in various cellular processes. This antibody, developed using advanced technology, exhibits high specificity and sensitivity in detecting LHFPL6 in human samples, making it a reliable choice for research studies. Validated for use in immunohistochemistry and flow cytometry, it enables precise localization and quantification of the LHFPL6 protein in different cell types.LHFPL6, also known as lipoma HMGIC fusion partner-like 6, is implicated in cell adhesion, signal transduction, and development, making it a key protein of interest in molecular biology and developmental biology research.
Its role in these pathways suggests its potential relevance in diseases such as cancer, neurological disorders, and genetic syndromes. By studying LHFPL6 expression and function, researchers can uncover valuable insights into disease mechanisms and potential therapeutic targets.
Antibody Name:
LHFPL6 Antibody (PACO27949)
Antibody SKU:
PACO27949
Size:
50ug
Host Species:
Rabbit
Tested Applications:
ELISA
Recommended Dilutions:
Species Reactivity:
Human
Immunogen:
Recombinant Human LHFPL tetraspan subfamily member 6 protein (31-83AA)
LHFPL tetraspan subfamily member 6 protein (Lipoma HMGIC fusion partner), LHFPL6, LHFP
UniProt Protein Function:
LHFP: A chromosomal aberration involving LHFP is associated with a subclass of benign mesenchymal tumors known as lipomas. Translocation t(12;13)(q13-q15;q12) with HMGA2 is shown in lipomas. Belongs to the LHFP family.Protein type: Membrane protein, multi-pass; Membrane protein, integralChromosomal Location of Human Ortholog: 13q12Molecular Function: DNA binding
UniProt Protein Details:
NCBI Summary:
This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. This gene is fused to a high-mobility group gene in a translocation-associated lipoma. Mutations in another LHFP-like gene result in deafness in humans and mice. Alternatively spliced transcript variants have been found; however, their full-length nature is not known. [provided by RefSeq, Jul 2008]
