Anti-Fig4/Sac3 Antibody (N202/7)

Our Anti-Fig4/Sac3 mouse monoclonal primary antibody from NeuroMab is produced in-house from hybridoma clone N202/7. It is KO validated, detects human and mouse Fig4/Sac3, and is purified by Protein A chromatography. It is great for use in IHC, ICC, WB.



SKU: 75-201

Volume: 100 µL
1-2 business days
Price:
Sale price$319.00

Product Specific References for Applications and Species

Immunohistochemistry: Mouse
PMID Dilution Publication
29518270not listedHu, B., et al. 2018. Myelin abnormality in Charcot-Marie-Tooth type 4J recapitulates features of acquired demyelination. Annals of Neurology, 756-770.
268079881:200Jones, J.M., et al. 2016. Single amino acid deletion in transmembrane segment D4S6 of sodium channel Scn8a (Nav1.6) in a mouse mutant with a chronic movement disorder. Neurobiology Disorders, 36-45.
22028665not listedVaccari, I., et al. 2011. Genetic interaction between MTMR2 and FIG4 phospholipid phosphatases involved in Charcot-Marie-Tooth neuropathies.. PLOS Genetics, e1002319.
Immunoprecipitation: Human
PMID Dilution Publication
265193810.4-10ug/mlCottarel, J., et al. 2016. FIG4 is a hepatitis C virus particle-bound protein implicated in virion morphogenesis and infectivity with cholesteryl ester modulation potential. Journal of General Virology, 69-81.
Western Blot: Human
PMID Dilution Publication
38725096not listedZhao, M, et al. 2024. Coxiella burnetii effector CvpE maintains biogenesis of Coxiella-containing vacuoles by suppressing lysosome tubulation through binding PI(3)P and perturbing PIKfyve activity on lysosomes. Virulence, 2350893.
31313076not listedShisheva, A., et al. 2019. Severe Consequences of SAC3/FIG4 Phosphatase Deficiency to Phosphoinositides in Patients with Charcot-Marie-Tooth Disease Type-4J. Molecular Neurobiology, 8656-8667.
28859335not listedGentil, B.J., et al. 2017. A New Mutation in FIG4 Causes a Severe Form of CMT4J Involving TRPV4 in the Pathogenic Cascade. Journal of Neuropathology and Experimental Neurology, 789-799.
25239001not listedde Kovel, C.G., et al. 2014. Characterization of a de novo SCN8A mutation in a patient with epileptic encephalopathy.. Epilepsy Research, 1511-1518.

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Western Blot: Mouse
PMID Dilution Publication
28859335not listedGentil, B.J., et al. 2017. A New Mutation in FIG4 Causes a Severe Form of CMT4J Involving TRPV4 in the Pathogenic Cascade. Journal of Neuropathology and Experimental Neurology, 789-799.
28552585not listedMorioka, S., et al. 2017. Phosphoinositide phosphatase Sac3 regulates the cell surface expression of scavenger receptor A and formation of lipid droplets in macrophages. Experimental Cell Research, 252-259.
270081791:200Mironova, Y.A., et al. 2016. PI (3, 5) P2 biosynthesis regulates oligodendrocyte differentiation by intrinsic and extrinsic mechanisms.. Elife, e13023.
25187576not listedVaccari, I., et al. 2015. Loss of Fig4 in both Schwann cells and motor neurons contributes to CMT4J neuropathy.. Human Molecular Genetics, 383-396.
24598713not listedBaulac, S.,, et al. 2014. Role of the phosphoinositide phosphatase FIG4 gene in familial epilepsy with polymicrogyria. Neurology, 1068-1075.
240045191:1000Reifler, A., et al. 2013. Murine Fig4 is dispensable for muscle development but required for muscle function.. Skelet Muscle., 21.
230476931:500Zolov, S.N., et al. 2012. In vivo, Pikfyve generates PI(3,5)P2, which serves as both a signaling lipid and the major precursor for PI5P.. PNAS USA, 17472-17477.
229984431:200Tahtouh, T., et al. 2012. Selectivity, cocrystal structures, and neuroprotective properties of leucettines, a family of protein kinase inhibitors derived from the marine sponge alkaloid leucettamine B.. Journal of Medicinal Chemistry, 9312-9330.
21872275not listedYan, Q., et al. 2012. Trauma does not accelerate neuronal degeneration in Fig4 insufficient mice.. Journal of the Neurological Sciences, 102-107.
216550881:200Lenk, G.M., et al. 2011. Pathogenic mechanism of the FIG4 mutation responsible for Charcot-Marie-Tooth disease CMT4J.. PLOS Genetics, e1002104.