The IMPG2 Antibody (PAC061546) is a valuable tool for researchers studying the IMPG2 protein, which plays a key role in maintaining the structure and function of the extracellular matrix in various tissues. This polyclonal antibody, produced in rabbits, exhibits high reactivity towards human samples and is validated for use in Western blot applications.IMPG2 is a crucial component in the development and maintenance of connective tissues, particularly in the eye where it contributes to the structure of the cornea and retina.
Research into IMPG2 is essential for understanding diseases such as macular degeneration and corneal dystrophies, which are associated with abnormalities in the extracellular matrix.By using the IMPG2 Antibody, researchers can detect and analyze IMPG2 expression in different cell types and tissues, providing valuable insights into its role in health and disease. This antibody is a valuable tool for studies in ophthalmology, developmental biology, and tissue engineering.
Antibody Name:
IMPG2 Antibody (PACO61546)
Antibody SKU:
PACO61546
Size:
50ug
Host Species:
Rabbit
Tested Applications:
ELISA, IF
Recommended Dilutions:
ELISA:1:2000-1:10000, IF:1:50-1:200
Species Reactivity:
Human
Immunogen:
Recombinant Human Interphotoreceptor matrix proteoglycan 2 protein (616-759AA)
Immunofluorescence staining of Hela cells with PACO61546 at 1:133, 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).
Background:
Chondroitin sulfate- and hyaluronan-binding proteoglycan involved in the organization of interphotoreceptor matrix; may participate in the maturation and maintenance of the light-sensitive photoreceptor outer segment. Binds heparin.
Synonyms:
Interphotoreceptor matrix proteoglycan 2, Interphotoreceptor matrix proteoglycan of 200 kDa, IPM 200, Sialoprotein associated with cones and rods proteoglycan, Spacrcan, IMPG2, IPM200
UniProt Protein Function:
IMPG2: Chondroitin sulfate- and hyaluronan-binding proteoglycan involved in the organization of interphotoreceptor matrix; may participate in the maturation and maintenance of the light- sensitive photoreceptor outer segment. Binds heparin. Defects in IMPG2 are the cause of retinitis pigmentosa type 56 (RP56). RP56 is a retinal dystrophy belonging to the group of pigmentary retinopathies. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. Defects in IMPG2 are the cause of maculopathy IMPG2- related (MACLP-IMPG2). MACLP-IMPG2 is a mild maculopathy characterized by full-field electroretinogram responses within normal limits, normal color vision, elevation of the photoreceptor layer in the foveal region and mild nuclear sclerosis.Protein type: Extracellular matrix; Membrane protein, integralChromosomal Location of Human Ortholog: 3q12.2-q12.3Cellular Component: proteinaceous extracellular matrix; integral to membrane; receptor complexMolecular Function: heparin binding; extracellular matrix structural constituent; hyaluronic acid bindingBiological Process: visual perceptionDisease: Retinitis Pigmentosa 56; Macular Dystrophy, Vitelliform, 5
UniProt Protein Details:
NCBI Summary:
The protein encoded by this gene binds chondroitin sulfate and hyaluronan and is a proteoglycan. The encoded protein plays a role in the organization of the interphotoreceptor matrix and may promote the growth and maintenance of the light-sensitive photoreceptor outer segment. Defects in this gene are a cause of retinitis pigmentosa type 56 and maculopathy, IMPG2-related.[provided by RefSeq, Mar 2011]