Host: |
Mouse |
Applications: |
IF/IHC |
Reactivity: |
Human/Horse |
Note: |
STRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS. |
Short Description: |
Mouse monoclonal antibody anti-Pmel17/gp100 is suitable for use in Immunofluorescence and Immunohistochemistry research applications. |
Clonality: |
Monoclonal |
Clone ID: |
EBS-O-147 |
Conjugation: |
Unconjugated |
Isotype: |
IgG2bk |
Formulation: |
PBS with 0.02% Sodium Azide. |
Purification: |
Affinity purified from tissue culture. |
Concentration: |
Can be provided as 100 µg/mL, 500 µg/mL or 1mg/mL. |
Dilution Range: |
Immunofluorescence on fixed cells (0, 5-1, 0 µg/ml). Immunohistology (1-2 µg/ml for 30 min at RT; staining of formalin-fixed tissues requires boiling tissue sections in 10mM citrate buffer, pH 6.0, for 10-20 min followed by cooling at RT for 20 minut |
Storage Instruction: |
Store for up to 1 year at 2-8°C upon receipt. |
Gene Symbol: |
PMEL |
Gene ID: |
6490 |
Uniprot ID: |
PMEL_HUMAN |
Immunogen: |
A BALB/c mouse was immunized with fresh metatstatic melanotic melanoma cell membranes. Fusion partner: SP-2/0. |
Post Translational Modifications | N- and O-glycosylated. A small amount of P1/P100 (major form) undergoes glycosylation in ER and Golgi compartments to yield P2/P120 (minor form). The mature P2 form leaves the trans-Golgi network and is mainly targeted to stage I melanosomes via the plasma membrane and clathrin-mediated endocytosis. Stage II melanosomes harbor only Golgi-modified fragments that are derived from M-alpha and that bear sialylated O-linked oligosaccharides. O-glycosylation of the RPT region is a conserved feature likely involved in amyloid sheet separation via electrostatic repulsion. Undergoes multiple proteolytic processing. In a post-Golgi prelysosomal compartment, P2 is cleaved by a furin-like proprotein convertase (PC) into two disulfide-linked subunits: a large lumenal subunit, M-alpha/ME20-S, and an integral membrane subunit, M-beta. Despite cleavage, only a small fraction of M-alpha is secreted, as most M-alpha and M-beta remain associated with each other intracellularly via a disulfide bond. Once targeted to stage I melanosomes, beta-secretase BACE2 cleaves the M-beta fragment to release the amyloidogenic luminal fragment containing M-alpha and a small portion of M-beta N-terminus. M-alpha is further cleaved by metalloproteinases, likely ADAM10 or ADAM17, and still unknown proteases to yield subfragments that ultimately assemble into amyloid fibrils. The C-terminal fragment of M-beta is processed by the gamma-secretase complex to release a short intracytoplasmic domain. |
Function | Forms physiological amyloids that play a central role in melanosome morphogenesis and pigmentation. The maturation of unpigmented premelanosomes from stage I to II is marked by assembly of processed amyloidogenic fragments into parallel fibrillar sheets, which elongate the vesicle into a striated ellipsoidal shape. In pigmented stage III and IV melanosomes, the amyloid matrix serves as a platform where eumelanin precursors accumulate at high local concentrations for pigment formation. May prevent pigmentation-associated toxicity by sequestering toxic reaction intermediates of eumelanin biosynthesis pathway. Represents a potent melanoma-specific antigen. Among melanoma non-mutated self-peptides, G9-154 (KTWGQYWQV), G9-209 (ITDQVPFSV) and G9-280 (YLEPGPVTA), appear to act as immunodominant common epitopes that stimulate anti-tumor immune response mediated by HLA-A-restricted cytotoxic T cells. |
Protein Name | Melanocyte Protein PmelMe20-MMe20mMelanocyte Protein Pmel 17Melanocytes Lineage-Specific Antigen Gp100Melanoma-Associated Me20 AntigenP1P100Premelanosome ProteinSilver Locus Protein Homolog Cleaved Into - M-Alpha95 Kda Melanocyte-Specific Secreted GlycoproteinP26Secreted Melanoma-Associated Me20 AntigenMe20-SMe20s - M-Beta |
Cellular Localisation | Endoplasmic Reticulum MembraneSingle-Pass Type I Membrane ProteinGolgi ApparatusCis-Golgi Network MembraneEndosomeMultivesicular BodyMelanosomeExtracellular VesicleSecretedIdentified By Mass Spectrometry In Melanosome Fractions From Stage I To Stage IvLocalizes Predominantly To Intralumenal Vesicles (Ilvs) Within Multivesicular BodiesAssociates With Ilvs Found Within The Lumen Of Premelanosomes And Melanosomes And Particularly In Compartments That Serve As Precursors To The Striated Stage Ii PremelanosomesSorted To Stage I Melanosomes Following Its Processing In The Er And Cis-GolgiTransiently Expressed At The Cell Surface Before Targeting To Early MelanosomesColocalizes With Bace2 In Stage I And Ii MelanosomesColocalizes With Cd63 And Apoe At Exosomes And In Intraluminal Vesicles Within Multivesicular Endosomes |
Alternative Antibody Names | Anti-Melanocyte Protein Pmel antibodyAnti-Me20-M antibodyAnti-Me20m antibodyAnti-Melanocyte Protein Pmel 17 antibodyAnti-Melanocytes Lineage-Specific Antigen Gp100 antibodyAnti-Melanoma-Associated Me20 Antigen antibodyAnti-P1 antibodyAnti-P100 antibodyAnti-Premelanosome Protein antibodyAnti-Silver Locus Protein Homolog Cleaved Into - M-Alpha antibodyAnti-95 Kda Melanocyte-Specific Secreted Glycoprotein antibodyAnti-P26 antibodyAnti-Secreted Melanoma-Associated Me20 Antigen antibodyAnti-Me20-S antibodyAnti-Me20s - M-Beta antibodyAnti-PMEL antibodyAnti-D12S53E antibodyAnti-PMEL17 antibodyAnti-SILV antibody |
Information sourced from Uniprot.org
12 months for antibodies. 6 months for ELISA Kits. Please see website T&Cs for further guidance