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IP for Anti-Netrin-1 [IPI-NTN1.43] in MCF7 culture medium

Addgene #241894

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 December 17, 2025)
DOI
https://doi.org/10.57733/addgene.qhitqd
Abstract
Experimental results for Anti-Netrin-1 [IPI-NTN1.43] (Addgene #241894) in an immunoprecipitation assay on MCF7 culture medium.
Citation
IP for Anti-Netrin-1 [IPI-NTN1.43] in MCF7 culture medium. Ayoubi R, González Bolívar S, Laflamme C 2025. Addgene Report, https://doi.org/10.57733/addgene.qhitqd
Caption: Culture medium was collected 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-NTN1.43] (Addgene #241894) pre-coupled to Dynabeads protein A. Samples were washed and processed for western blot with the 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-NTN1.43]
Addgene #241894

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-NTN1.43]
Source
Addgene
Catalog Number
241894
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