HDAC6 Antibody - BSA Free
Novus Biologicals | Catalog # NBP1-78981
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Scientific Data Images for HDAC6 Antibody - BSA Free
Immunocytochemistry/ Immunofluorescence: HDAC6 Antibody - BSA Free [NBP1-78981]
Immunocytochemistry/Immunofluorescence: HDAC6 Antibody [NBP1-78981] - HDAC-6 antibody was tested in HeLa cells with FITC (green). Nuclei and alpha-tubulin were counterstained with DAPI (blue) and DyLight 550 (red).Flow Cytometry: HDAC6 Antibody - BSA Free [NBP1-78981]
Flow Cytometry: HDAC6 Antibody [NBP1-78981] - Analysis using the Alexa Fluor (R) 488 conjugate of NBP1-78981. Staining of isolated T-cells. Image from verified customer review (Andressa Sodre, Moffitt Cancer Center).Applications for HDAC6 Antibody - BSA Free
Immunocytochemistry/ Immunofluorescence
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Background: Histone Deacetylase 6/HDAC6
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Additional Histone Deacetylase 6/HDAC6 Products
Product Documents for HDAC6 Antibody - BSA Free
Certificate of Analysis
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Product Specific Notices for HDAC6 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.
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Protocols
View specific protocols for HDAC6 Antibody - BSA Free (NBP1-78981):
Immunocytochemistry Protocol
Culture cells to appropriate density in 35 mm culture dishes or 6-well plates.
1. Remove culture medium and add 10% formalin to the dish. Fix at room temperature for 30 minutes.
2. Remove the formalin and add ice cold methanol. Incubate for 5-10 minutes.
3. Remove methanol and add washing solution (i.e. PBS). Be sure to not let the specimen dry out. Wash three times for 10 minutes.
4. To block nonspecific antibody binding incubate in 10% normal goat serum from 1 hour to overnight at room temperature.
5. Add primary antibody at appropriate dilution and incubate at room temperature from 2 hours to overnight at room temperature.
6. Remove primary antibody and replace with washing solution. Wash three times for 10 minutes.
7. Add secondary antibody at appropriate dilution. Incubate for 1 hour at room temperature.
8. Remove antibody and replace with wash solution, then wash for 10 minutes. Add Hoechst 33258 to wash solution at 1:25,0000 and incubate for 10 minutes. Wash a third time for 10 minutes.
9. Cells can be viewed directly after washing. The plates can also be stored in PBS containing Azide covered in Parafilm (TM). Cells can also be cover-slipped using Fluoromount, with appropriate sealing.
*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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