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IP for Anti-Netrin-1 [IPI-NTN1.65] in MCF7 culture medium

Addgene #241895

Data Submitted By
Riham Ayoubi, Sara González Bolívar and Carl Laflamme
Lab Name
Carl Laflamme, YCharOS
Submission Date
November 18, 2025
Publication Date
November 26, 2025 (modified August 20, 2026)
DOI
https://doi.org/10.57733/addgene.4gukp7
Abstract
Experimental results for Anti-Netrin-1 [IPI-NTN1.65] (Addgene #241895) in an immunoprecipitation assay on MCF7 culture medium.
Citation
IP for Anti-Netrin-1 [IPI-NTN1.65] in MCF7 culture medium. Ayoubi R, González Bolívar S, Laflamme C 2025. Addgene Report, https://doi.org/10.57733/addgene.4gukp7
Caption: Culture medium was collected from from a MCF7 cell culture, and immunoprecipitation was performed for 1 h using 0.15 mg of protein and 2 µg of Anti-Netrin-1 [IPI-NTN1.65] (Addgene #241895) pre-coupled to Dynabeads protein A. Samples were washed and processed for western blot with Anti-Netrin 1 antibody [EPR5428] (Abcam #ab126729) diluted at 1/2000. The Ponceau stained transfers of each blot are shown. SM: 10% starting material; UB: 10% unbound fraction; IP: immunoprecipitate, HC: antibody heavy chain.
Image attribution: Carl Laflamme, YCharOS

This report is made available under the Creative Commons Attribution 4.0 International License.

Antibody Used
Anti-Netrin-1 [IPI-NTN1.65]
Addgene #241895

Materials & Methods

Sample

Target Species
Human
Cell / Tissue Type
MCF7 breast adenocarcinoma cells
Total Amount
0.15 mg

Matrix

Type of Immobilization
Protein A
Amount
30 µL

Primary Antibody

Name
Anti-Netrin-1 [IPI-NTN1.65]
Source
Addgene
Catalog Number
241895
Host Species
Rabbit
Target Antigen
NTN1
Concentration
2 µg
Time
60 min
Temperature
4 ˚C
View in Addgene Catalog

Additional Information

Additional Information

Publication

Ayoubi et al. (2025). A guide to selecting high-performing antibodies for Netrin-1 (UniProt ID: O95631) for use in western blot and immunoprecipitation. Zenodo. Download article (Link opens in a new window)

Protocol

Antibody-bead conjugates were prepared by adding 2 µg of antibody to 500 µL of Pierce IP Lysis Buffer (25 mM Tris-HCl pH 7.4, 150 mM NaCl, 1 mM EDTA, 1% NP-40 and 5% glycerol; Thermo Fisher Scientific #87788) in a microcentrifuge tube, together with 30 µL of Dynabeads protein A (Thermo Fisher Scientific #10002D). Tubes were rocked for ~1 h at 4 °C followed by two washes to remove unbound antibodies. Culture media from WT MCF7 were collected and total protein quantified. Aliquots of 0.15 mL of culture medium, containing 1 mg/mL total protein, were incubated with the antibody-bead conjugate for ~1 h at 4 °C. The unbound fractions were collected, and beads were subsequently washed three times with 1 mL of IP buffer and processed for SDS-PAGE and western blot on precast midi 4–20% Tris-Glycine polyacrylamide gels. Protein A:HRP was used as a secondary detection system at a concentration of 0.5 µg/mL.

Detection Assay
Western blot
Predicted Molecular Weight
67.5 kDa

Results

Result
Pass (The antibody worked under these conditions)
Describe Results
Strong signal