Human CLN3 protein (Recombinant) (N-GST & C-His) (STJP008512)

SKU:
STJP008512
€410.63 - €1,796.88
Free Shipping
Processing The item has been added

Host: E. coli
Note: STRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.
Short Description : Recombinant-Human CLN3-N-GST & C-His protein was developed from e. coli and has a target region of N-GST & C-His. For use in research applications.
Formulation: Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.
Storage Instruction: Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at-20 to-80°C for twelve months from the date of receipt.
Gene Symbol: CLN3
Gene ID: 1201
Uniprot ID: CLN3_HUMAN
Immunogen Region: Gln204-Val277
Immunogen: Homo sapiens (Human)
Post Translational Modifications Highly glycosylated. Farnesylation is important for trafficking to lysosomes. Phosphorylated on both serine and threonine residues by PKA, PKG and CK2.
Function Mediates microtubule-dependent, anterograde transport connecting the Golgi network, endosomes, autophagosomes, lysosomes and plasma membrane, and participates in several cellular processes such as regulation of lysosomal pH, lysosome protein degradation, receptor-mediated endocytosis, autophagy, transport of proteins and lipids from the TGN, apoptosis and synaptic transmission. Facilitates the proteins transport from trans-Golgi network (TGN)-to other membrane compartments such as transport of microdomain-associated proteins to the plasma membrane, IGF2R transport to the lysosome where it regulates the CTSD release leading to regulation of CTSD maturation and thereby APP intracellular processing. Moreover regulates CTSD activity in response to osmotic stress. Also binds galactosylceramide and transports it from the trans Golgi to the rafts, which may have immediate and downstream effects on cell survival by modulating ceramide synthesis. At the plasma membrane, regulates actin-dependent events including filopodia formation, cell migration, and pinocytosis through ARF1-CDC42 pathway and also the cytoskeleton organization through interaction with MYH10 and fodrin leading to the regulation of the plasma membrane association of Na+, K+ ATPase complex. Regulates synaptic transmission in the amygdala, hippocampus, and cerebellum through regulation of synaptic vesicles density and their proximity to active zones leading to modulation of short-term plasticity and age-dependent anxious behavior, learning and memory. Regulates autophagic vacuoles (AVs) maturation by modulating the trafficking between endocytic and autophagolysosomal/lysosomal compartments, which involves vesicle fusion leading to regulation of degradation process. Participates also in cellular homeostasis of compounds such as, water, ions, amino acids, proteins and lipids in several tissue namely in brain and kidney through regulation of their transport and synthesis.
Protein Name Battenin
Batten Disease Protein
Protein Cln3
Database Links Reactome: R-HSA-9845576
Cellular Localisation Lysosome Membrane
Multi-Pass Membrane Protein
Late Endosome
Lysosome
Golgi Apparatus
Golgi Apparatus Membrane
Golgi Stack
Trans-Golgi Network
Cell Membrane
Recycling Endosome
Membrane Raft
Membrane
Caveola
Early Endosome Membrane
Synapse
Synaptosome
Late Endosome Membrane
Cytoplasmic Vesicle
Autophagosome
Cln3 Is Not Present In Late Endosomes/Lysosomes In Fibroblasts And Neurons
Trafficks From Cell Membrane To Golgi Via Endosomes
Osmotic Stress Changes The Subcellular Localization Of Cln3
Trafficks To Intracellular Compartments Via The Plasma Membranet Through Ap3m1-Dependent Mechanisms
Excluded From The Synaptic Vesicles
Alternative Protein Names Battenin protein
Batten Disease Protein protein
Protein Cln3 protein
CLN3 protein
BTS protein

Information sourced from Uniprot.org