The LPAR6 Antibody (PAC063687) is a valuable tool for researchers studying LPAR6, a G protein-coupled receptor known to be involved in various cellular processes, including cell migration and differentiation. This polyclonal antibody, produced in rabbits, is highly specific and reacts with human samples, providing reliable results in Western blot applications.LPAR6, also known as lysophosphatidic acid receptor 6, has been implicated in a range of physiological and pathological conditions, such as cancer progression, neuropathic pain, and cardiovascular disease. By targeting LPAR6, researchers can gain insights into the molecular mechanisms underlying these conditions and potentially identify novel therapeutic targets for intervention.
With its high specificity and reliability, the LPAR6 Antibody is an essential tool for investigating the role of LPAR6 in various biological processes and disease states. Whether studying cell signaling pathways, drug development, or disease mechanisms, this antibody offers researchers a valuable resource for advancing their research in the fields of biochemistry, pharmacology, and cell biology.
Western Blot. Positive WB detected in: Hela whole cell lysate, A549 whole cell lysate, HepG2 whole cell lysate, PC-3 whole cell lysate. All lanes: LPAR6 antibody at 1:2000. Secondary. Goat polyclonal to rabbit IgG at 1/50000 dilution. Predicted band size: 40 kDa. Observed band size: 40 kDa.
Immunofluorescence staining of HepG2 cells with PACO63687 at 1:100, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).
IHC image of PACO63687 diluted at 1:200 and staining in paraffin-embedded human colon cancer performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.
Background:
Binds to oleoyl-L-alpha-lysophosphatidic acid, (LPA). Intracellular cAMP is involved in the receptor activation. Important for the maintenance of hair growth and texture.
P2RY5: Binds to oleoyl-L-alpha-lysophosphatidic acid (LPA). Intracellular cAMP is involved in the receptor activation. Important for the maintenance of hair growth and texture. Defects in LPAR6 are the cause of woolly hair autosomal recessive type 1 with or without hypotrichosis (ARWH1). A hair shaft disorder characterized by fine and tightly curled hair. Compared to normal curly hair that is observed in some populations, woolly hair grows slowly and stops growing after a few inches. Under light microscopy, woolly hair shows some structural anomalies, including trichorrhexis nodosa and tapered ends. Defects in LPAR6 are the cause of hypotrichosis type 8 (HYPT8). A condition characterized by the presence of less than the normal amount of hair. Affected individuals show progressive hair loss, thinning of scalp hair since early childhood, sparse body hair, and sparse eyebrows and eyelashes in some cases. Belongs to the G-protein coupled receptor 1 family.Protein type: Receptor, GPCR; Membrane protein, integral; GPCR, family 1; Membrane protein, multi-passChromosomal Location of Human Ortholog: 13q14Cellular Component: plasma membrane; integral to membraneMolecular Function: G-protein coupled receptor activityBiological Process: G-protein coupled receptor protein signaling pathwayDisease: Hypotrichosis 8
UniProt Protein Details:
NCBI Summary:
The protein encoded by this gene belongs to the family of G-protein coupled receptors, that are preferentially activated by adenosine and uridine nucleotides. This gene aligns with an internal intron of the retinoblastoma susceptibility gene in the reverse orientation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2009]