IP for Anti-Netrin-1 [IPI-NTN1.33] in MCF7 culture medium
Addgene #241893
- 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.huw20c
- Abstract
- Experimental results for Anti-Netrin-1 [IPI-NTN1.33] (Addgene #241893) in an immunoprecipitation assay on MCF7 culture medium.
- Citation
-
IP for Anti-Netrin-1 [IPI-NTN1.33] in MCF7 culture medium. Ayoubi R, González Bolívar S, Laflamme C 2025. Addgene Report, https://doi.org/10.57733/addgene.huw20c
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-NTN1.33]
Addgene #241893
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-NTN1.33]
- Source
- Addgene
- Catalog Number
- 241893
- Host Species
- Rabbit
- Target Antigen
- NTN1
- Concentration
- 2 µg
- Time
- 60 min
- Temperature
- 4 ˚C
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