JMJD2D Antibody - BSA Free
Novus Biologicals | Catalog # NBP1-03357
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Key Product Details
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Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Scientific Data Images for JMJD2D Antibody - BSA Free
Western Blot: JMJD2D AntibodyBSA Free [NBP1-03357]
Western Blot: JMJD2D Antibody [NBP1-03357] - Western Blot Image of anti-JMJD2D. Whole cell protein from PC3 (lane 1), SHSY5Y (lane 2), and HeLa (lane 3) was separated on a 12% gel by SDS-PAGE, transferred to PVDF membrane and blocked in 5% non-fat milk in TBST. The membrane was probed with 2.0 ug/ml anti-JMJD2D in 1% milk, and detected with an anti-rabbit HRP secondary antibody using chemiluminescence.Applications for JMJD2D Antibody - BSA Free
Chromatin Immunoprecipitation
Western Blot
Reviewed Applications
Read 2 reviews rated 5 using NBP1-03357 in the following applications:
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Background: JMJD2D
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Additional JMJD2D Products
Product Documents for JMJD2D Antibody - BSA Free
Certificate of Analysis
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Product Specific Notices for JMJD2D Antibody - BSA Free
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
Citations for JMJD2D Antibody - BSA Free
Customer Reviews for JMJD2D Antibody - BSA Free (2)
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Application: Western BlotSample Tested: glioblastoma cell lysates and primary cancer cellsSpecies: HumanVerified Customer | Posted 03/25/201925 ug of lysate loaded per well (0.8 ug/uL) of naive vs treated FPW1 primary glioblastoma cells. Three independent repeat-pairs are shown. Exposure of about 1 min.Bolt system (Life Technologies) was used. Prior to running the gel, DTT was added to the samples and samples were heated for 5 min at 95 degrees Celsius and rapidly cooled on ice.
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Application: Western BlotSample Tested: MDA-MB-435 cell lysatesSpecies: HumanVerified Customer | Posted 01/11/2012
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Protocols
View specific protocols for JMJD2D Antibody - BSA Free (NBP1-03357):
Western Blot Protocol
1. Perform SDS-PAGE (4-12% MOPS) on samples to be analyzed, loading 30 ug of total protein per lane.
2. Transfer proteins to Nitrocellulose according to the instructions provided by the manufacturer of the transfer
apparatus.
3. Rinse membrane with dH2O and then stain the blot using Ponceau S for 1-2 minutes to access the transfer of proteins onto the nitrocellulose membrane. Rinse the blot in water to remove excess stain and mark the lane locations and locations of molecular weight markers using a pencil.
4. Rinse the blot in TBS for approximately 5 minutes.
5. Block the membrane using 5% BSA in TBS + Tween, 1 hour at RT.
6. Rinse the membrane in dH2O and then wash the membrane in wash buffer [TBS + 0.1% Tween] 3 times for 10 minutes each.
7. Dilute the rabbit anti-JMJD2D primary antibody (NBP1-03357) in blocking buffer and incubate 1 hour at room temperature.
8. Rinse the membrane in dH2O and then wash the membrane in wash buffer [TBS + 0.1% Tween] 3 times for 10 minutes each.
9. Apply the diluted rabbit-IgG HRP-conjugated secondary antibody in blocking buffer (as per manufacturers
instructions) and incubate 1 hour at room temperature.
10. Wash the blot in wash buffer [TBS + 0.1% Tween] 3 times for 10 minutes each (this step can be repeated as required to reduce background).
11. Apply the detection reagent of choice in accordance with the manufacturers instructions (Pierce ECL).
Note: Tween-20 can be added to the blocking or antibody dilution buffer at a final concentration of 0.05-0.2%, provided it does not interfere with antibody-antigen binding.
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
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- Troubleshooting Guide: Western Blot Figures
- Western Blot Conditions
- Western Blot Protocol
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- Western Blot Troubleshooting
- Western Blot Troubleshooting Guide
- View all Protocols, Troubleshooting, Illustrated assays and Webinars