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Scientific Data Images for SETD8 Antibody - BSA Free
Western Blot: SETD8 AntibodyBSA Free [NBP1-91269]
Western Blot: SETD8 Antibody [NBP1-91269] - Analysis of SETD8 in whole cell lysates of mouse proliferating neural progenitors (P) and differentiating neural stem cell (D) using anti-SETD8 antibody. Image from verified customer review.Western Blot: SETD8 AntibodyBSA Free [NBP1-91269]
Western Blot: SETD8 Antibody [NBP1-91269] - Western blot analysis of SETD8 in Lane 1. SETD8 overexpression vector containing C-terminal DDK tag. Lane 2. Empty vector.Applications for SETD8 Antibody - BSA Free
Western Blot
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Read 2 reviews rated 5 using NBP1-91269 in the following applications:
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Background: SETD8
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Product Documents for SETD8 Antibody - BSA Free
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Product Specific Notices for SETD8 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.
Customer Reviews for SETD8 Antibody - BSA Free (2)
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Application: Western BlotSample Tested: Whole cell lysate of mouse neural progenitors proliferating and differentiated for 24 hr.Species: MouseVerified Customer | Posted 06/09/2016Expression of SETD8 in proliferating neural progenitors (P) and differentiatiating neural stem cell (D).
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Application: Western BlotSample Tested: Cell lysate from HCT116 cells grown in DMEM mediumSpecies: HumanVerified Customer | Posted 10/09/2014SETD8 immunoblot in Jurkat cells
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Protocols
View specific protocols for SETD8 Antibody - BSA Free (NBP1-91269):
Western Blot Protocol
1. Perform SDS-PAGE on samples to be analyzed, loading 40 ug of total protein per lane.
2. Transfer proteins to membrane according to the instructions provided by the manufacturer of the membrane and transfer apparatus.
3. Stain according to standard Ponceau S procedure (or similar product) to assess transfer success, and mark molecular weight standards where appropriate.
4. Rinse the blot.
5. Block the membrane using standard blocking buffer for at least 1 hour.
6. Wash the membrane in wash buffer three times for 10 minutes each.
7. Dilute primary antibody in blocking buffer and incubate 1 hour at room temperature.
8. Wash the membrane in wash buffer three times for 10 minutes each.
9. Apply the diluted 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 three 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.
Note: Tween-20 can be added to the blocking or antibody dilution buffer at a final concentration of 0.05-0.2%..
*The above information is only intended as a guide. The researcher should determine what protocol best meets their needs. Please follow safe laboratory procedures.
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