Mouse Anti-CYFIP2 Recombinant Antibody (4G6) (V2LY-0125-LY874)

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Basic Information

Host Animal
Mouse
Clone
4G6
Application
ELISA, WB
Immunogen
CYFIP2 (733-820aa) partial recombinant protein.
Host Species
Mouse
Specificity
Human
Antibody Isotype
IgG2a, κ
Clonality
Monoclonal Antibody

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
PBS
Preservative
None
Concentration
Batch dependent
Purity
>95% as determined by analysis by SDS-PAGE
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freezethaw cycles.
More Infomation

Target

Full Name
cytoplasmic FMR1 interacting protein 2
Entrez Gene ID
UniProt ID
Function
Involved in T-cell adhesion and p53/TP53-dependent induction of apoptosis. Does not bind RNA. As component of the WAVE1 complex, required for BDNF-NTRK2 endocytic trafficking and signaling from early endosomes (By similarity).
Biological Process
Activation of cysteine-type endopeptidase activity Source: BHF-UCL
Apoptotic process Source: UniProtKB
Cell-cell adhesion Source: UniProtKB
Cell morphogenesis Source: GO_Central
Fc-gamma receptor signaling pathway involved in phagocytosis Source: Reactome
Positive regulation of proteolysis Source: BHF-UCL
Regulation of actin filament polymerization Source: InterPro
Vascular endothelial growth factor receptor signaling pathway Source: Reactome
Cellular Location
Cytoplasm; Nucleus; Perinuclear region; Synaptosome. Highly expressed in the perinuclear regionand enriched in synaptosomes (By similarity). Treatment with leptomycin-B triggers translocation to the nucleus (PubMed:17245118).
Involvement in disease
Developmental and epileptic encephalopathy 65 (DEE65):
A form of epileptic encephalopathy, a heterogeneous group of severe childhood onset epilepsies characterized by refractory seizures, neurodevelopmental impairment, and poor prognosis. Development is normal prior to seizure onset, after which cognitive and motor delays become apparent. DEE65 is an autosomal dominant form characterized by onset of intractable seizures usually in the first 6 months of life and severe to profound psychomotor developmental delay.

Manigandan, S., & Yun, J. W. (2022). Loss of cytoplasmic FMR1‐interacting protein 2 (CYFIP2) induces browning in 3T3‐L1 adipocytes via repression of GABA‐BR and activation of mTORC1. Journal of Cellular Biochemistry.

Chaya, T., Ishikane, H., Varner, L. R., Sugita, Y., Maeda, Y., Tsutsumi, R., ... & Furukawa, T. (2022). Deficiency of the neurodevelopmental disorder-associated gene Cyfip2 alters the retinal ganglion cell properties and visual acuity. Human molecular genetics, 31(4), 535-547.

Lee, Y., Zhang, Y., Kang, H., Bang, G., Kim, Y., Kang, H. R., ... & Han, K. (2020). Epilepsy-and intellectual disability-associated CYFIP2 interacts with both actin regulators and RNA-binding proteins in the neonatal mouse forebrain. Biochemical and biophysical research communications, 529(1), 1-6.

Zweier, M., Begemann, A., McWalter, K., Cho, M. T., Abela, L., Banka, S., ... & Rauch, A. (2019). Spatially clustering de novo variants in CYFIP2, encoding the cytoplasmic FMRP interacting protein 2, cause intellectual disability and seizures. European Journal of Human Genetics, 27(5), 747-759.

Zhang, Y., Lee, Y., & Han, K. (2019). Neuronal function and dysfunction of CYFIP2: from actin dynamics to early infantile epileptic encephalopathy. BMB reports, 52(5), 304.

Zhang, Y., Kang, H. R., & Han, K. (2019). Differential cell-type-expression of CYFIP1 and CYFIP2 in the adult mouse hippocampus. Animal cells and systems, 23(6), 380-383.

Zhang, Y., Kang, H., Lee, Y., Kim, Y., Lee, B., Kim, J. Y., ... & Han, K. (2019). Smaller body size, early postnatal lethality, and cortical extracellular matrix-related gene expression changes of Cyfip2-null embryonic mice. Frontiers in molecular neuroscience, 11, 482.

Cioni, J. M., Wong, H. H. W., Bressan, D., Kodama, L., Harris, W. A., & Holt, C. E. (2018). Axon-axon interactions regulate topographic optic tract sorting via CYFIP2-dependent WAVE complex function. Neuron, 97(5), 1078-1093.

Kirkpatrick, S. L., Goldberg, L. R., Yazdani, N., Babbs, R. K., Wu, J., Reed, E. R., ... & Bryant, C. D. (2017). Cytoplasmic FMR1-interacting protein 2 is a major genetic factor underlying binge eating. Biological psychiatry, 81(9), 757-769.

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For research use only. Not intended for any clinical use.

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