Mouse Recombinant KIRREL3 protein, His Tag (V2LY-0526-LY8592)

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Basic Information

Expressed Host
HEK293 Cells
Protein Species
Mouse
Tag
His Tag
Protein Construction
This product is Mouse Recombinant KIRREL3 protein, His Tag consist of Amino Acid: 1-535 and predicts a molecular mass of 57.5 kDa.
Molecule Mass
57.5 kDa
Sequence
Amino Acid: 1-535
Species
Mouse

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

Purity
>96% as determined by SDS-PAGE
Endotoxin
Please contact us for more information.
Format
Lyophilized
Reconstitution
Allow the vial and reconstitution buffer to equilibrate to room temperature. Briefly centrifuge or tap down the vial to ensure that all lyophilized powder is collected at the bottom of the vial. For the reconstitution of this product, we recommend adding PBS or sterile water to achieve a final antibody concentration of 1 mg/mL. Allow the vial to reconstitute for 10-15 minutes at room temperature with gentle agitation. Avoid vigorous shaking that can cause foaming and antibody denaturation. Aliquot into volumes based on your experiment and store liquid protein at -20°C or -80°C for long time.
Buffer
Lyophilized from sterile Sodium Citrate, NaCl, Tween80, Trehalose
Preservative
None
Storage
Samples are stable for up to twelve months from date of receipt at -20°C to -80°C. Store it under sterile conditions at -20°C to -80°C. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
More Infomation

Target

Full Name
kin of IRRE like 3 (Drosophila)
Function
Synaptic adhesion molecule required for the formation of target-specific synapses. Required for formation of target-specific synapses at hippocampal mossy fiber synapses. Required for formation of mossy fiber filopodia, the synaptic structures connecting dentate granule and GABA neurons. Probably acts as a homophilic adhesion molecule that promotes trans-cellular interactions and stabilize mossy fiber filipodia contact and subsequent synapse formation. Required for the coalescence of vomeronasal sensory neuron axons. May be involved in the hematopoietic supportive capacity of stroma cells; the secreted extracellular domain is directly responsible for supporting hematopoietic stem cells.
Biological Process
Cell-cell adhesionManual Assertion Based On ExperimentIBA:GO_Central
Glomerulus morphogenesisIEA:Ensembl
HemopoiesisISS:UniProtKB
Hippocampus developmentISS:UniProtKB
Homophilic cell adhesion via plasma membrane adhesion moleculesISS:UniProtKB
Inter-male aggressive behaviorIEA:Ensembl
Neuron migrationIEA:Ensembl
Neuron projection morphogenesisIEA:Ensembl
Principal sensory nucleus of trigeminal nerve developmentIEA:Ensembl
Synapse assemblyISS:UniProtKB
Cellular Location
Cell membrane
Processed kin of IRRE-like protein 3: Secreted
Involvement in disease
A chromosomal aberration involving KIRREL3 and CDH15 is found in a patient with severe mental retardation and dysmorphic facial features. Translocation t(11;16)(q24.2;q24).
Topology
Extracellular: 22-535
Helical: 536-556
Cytoplasmic: 557-778
PTM
Undergoes proteolysis by a metalloprotease and gives rise to a soluble form.

Querzani, A., Sirchia, F., Rustioni, G., Rossi, A., Orsini, A., Marseglia, G. L., ... & Foiadelli, T. (2023). KIRREL3-related disorders: a case report confirming the radiological features and expanding the clinical spectrum to a less severe phenotype. Italian Journal of Pediatrics, 49(1), 99.

Traenkner, D., Shennib, O., Johnson, A., Weinbrom, A., Taylor, M. R., & Williams, M. E. (2023). Modular Splicing is Linked to Evolution in the Synapse-Specificity Molecule Kirrel3. eNeuro.

Yang, B., Zhang, X., Zhou, H., Zhang, X., Yang, W., Lu, J., ... & Tian, F. (2022). Preliminary study on the role and mechanism of KIRREL3 in the development of esophageal squamous cell carcinoma. Pathology-Research and Practice, 237, 154025.

Ciaccio, C., Leonardi, E., Polli, R., Murgia, A., D'Arrigo, S., Granocchio, E., ... & Esposito, S. (2021). A missense de novo variant in the CASK-interactor KIRREL3 gene leading to neurodevelopmental disorder with mild cerebellar hypoplasia. Neuropediatrics, 52(06), 484-488.

Taylor, M. R., Martin, E. A., Sinnen, B., Trilokekar, R., Ranza, E., Antonarakis, S. E., & Williams, M. E. (2020). Kirrel3-mediated synapse formation is attenuated by disease-associated missense variants. Journal of Neuroscience, 40(28), 5376-5388.

Völker, L. A., Maar, B. A., Pulido Guevara, B. A., Bilkei‐Gorzo, A., Zimmer, A., Brönneke, H., ... & Hoehne, M. (2018). Neph2/Kirrel3 regulates sensory input, motor coordination, and home‐cage activity in rodents. Genes, Brain and Behavior, 17(8), e12516.

Hisaoka, T., Komori, T., Kitamura, T., & Morikawa, Y. (2018). Abnormal behaviours relevant to neurodevelopmental disorders in Kirrel3-knockout mice. Scientific Reports, 8(1), 1408.

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

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