anti neuropilin 1 nrp1 extracellular antibody (Alomone Labs)


Structured Review

Anti Neuropilin 1 Nrp1 Extracellular Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 93/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti neuropilin 1 nrp1 extracellular antibody/product/Alomone Labs
Average 93 stars, based on 2 article reviews
Price from $9.99 to $1999.99
Images
1) Product Images from "Giant ankyrin-B mediates transduction of axon guidance and collateral branch pruning factor Sema 3A"
Article Title: Giant ankyrin-B mediates transduction of axon guidance and collateral branch pruning factor Sema 3A
Journal: bioRxiv
doi: 10.1101/2021.05.03.442401

Figure Legend Snippet: AnkB440 stabilizes the Sema 3A receptor complex L1CAM-Nrp1 at the cell surface of GCs. ( A ) Western blot analysis of the expression of Sema 3A, L1CAM and the Sema 3A receptors Nrp1 and Plexin A1 in the cortex of PND1 control and AnkB440 KO mice. ( B ) Quantification of protein levels normalized to actin in cortical lysates from PND1 mice of indicated genotypes relative to their levels in control brains. Data show mean ± SEM for three biological replicates per genotype. Unpaired t test. *p
Techniques Used: Western Blot, Expressing, Mouse Assay
2) Product Images from "Giant ankyrin-B mediates transduction of axon guidance and collateral branch pruning factor sema 3A"
Article Title: Giant ankyrin-B mediates transduction of axon guidance and collateral branch pruning factor sema 3A
Journal: eLife
doi: 10.7554/eLife.69815

Figure Legend Snippet: Proposed mechanism of AnkB440-mediated growth cone collapse. AnkB440 binds the cytoplasmic domain of L1CAM to stabilize the L1CAM-Nrp1 holoreceptor complex at the cell surface. Transduction of Sema 3 A signals via the AnkB440-L1CAM-Nrp1 complex modulates F-actin dynamics through LIMK phosphorylation of cofilin to facilitate local F-actin disassembly and the collapse of GCs from the axon and collateral branches independently of βII-spectrin, or of AnkB440 interaction with microtubules. Source data . Source data contain the original files of the full raw unedited gels or blots and figures with the uncropped gels or blots with the relevant bands clearly labelled. Source data files also include numerical data that are represented as graphs in the figures.
Techniques Used: Transduction