ARG44971

anti-TRIM72 / MG53 antibody

anti-TRIM72 / MG53 antibody for IHC-Formalin-fixed paraffin-embedded sections and Human

Overview

Product Description Mouse Monoclonal antibody recognizes TRIM72 / MG53
Tested Reactivity Hu
Tested Application IHC-P
Host Mouse
Clonality Monoclonal
Isotype IgG1
Target Name TRIM72 / MG53
Antigen Species Human
Epitope FRALMPALEE LTFDPSSAHP SLVVSSSGRR VECSEQKAPP AGEDPRQFDK AVAVVAHQQL SEGEHYWEVD VGDKPRWALG VIAAEAPRRG RLHAVPSQGL WLLGLREGKI LEAHVEAKEP RALRSPERRP TRIGLYLSFG DGVLSFYDAS DADALVPLFA FHERLPRPVY PFFDVCWHDK GKNAQPLLLV
Conjugation Un-conjugated
Alternate Names TRIM72; Tripartite Motif Containing 72; MG53; Tripartite Motif Containing 72, E3 Ubiquitin Protein Ligase; Tripartite Motif-Containing Protein 72; Mitsugumin-53; Tripartite Motif-Containing 72; Mitsugumin 53; Mg53

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-P1:1000
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Protein A purification
Buffer PBS with 0.09% sodium azide
Preservative 0.09% sodium azide
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Gene Symbol TRIM72
Gene Full Name Tripartite Motif Containing 72
Background Enables identical protein binding activity. Predicted to be involved in several processes, including cellular protein metabolic process; plasma membrane repair; and protein homooligomerization. Predicted to act upstream of or within negative regulation of insulin receptor signaling pathway; negative regulation of insulin-like growth factor receptor signaling pathway; and negative regulation of myotube differentiation. Predicted to be located in cytoplasmic vesicle membrane. Predicted to be active in cytoplasm and sarcolemma. [provided by Alliance of Genome Resources, Apr 2022]
Function Muscle-specific protein that plays a central role in cell membrane repair by nucleating the assembly of the repair machinery at injury sites. Specifically binds phosphatidylserine. Acts as a sensor of oxidation: upon membrane damage, entry of extracellular oxidative environment results in disulfide bond formation and homooligomerization at the injury site. This oligomerization acts as a nucleation site for recruitment of TRIM72-containing vesicles to the injury site, leading to membrane patch formation. Probably acts upstream of the Ca2+-dependent membrane resealing process. Required for transport of DYSF to sites of cell injury during repair patch formation. Regulates membrane budding and exocytosis. May be involved in the regulation of the mobility of KCNB1-containing endocytic vesicles. [Uniprot]
Cellular Localization Cell membrane, Cytoplasmic vesicle, Membrane. [Uniprot]
PTM Disulfide bond, Phosphoprotein, S-nitrosylation. [Uniprot]