Description: 5-bromodeoxyuridine (BrdU) is an analogue of thymidine. When incubated with tissue, proliferating cells incorporate BrdU into the DNA during S phase and this provides an accurate means of determining cell proliferation. This antibody detects incorporated BrdU in cells or tissues.
Primary Antibody
Name: BrdU Antibody |
Clone: 85-2C8, Mouse anti-BrdU |
Supplier: Vector Labs |
Catalog Number: VP-B209 |
Dilution: 1:200 - 1:400 using IHC-TekTM Antibody Diluent (Cat# IW-1000 or IW-1001) to reduce background and unspecific staining and serum blocking step is NOT needed. |
Incubation Time/Temp: 60min/room temperature |
Device: IHC-TekTM Epitope Retrieval Steamer Set (Cat# IW-1102) |
Buffer/pH value: IHC-TekTM Epitope Retrieval Solution (Cat# IW-1100) or 2N HCl (see Note below for details) |
Heat/Cool Temperature: 95-100 ºC/room temperature |
Heat/Cool Time: 20 minutes/20 minutes |
Standard Method: ABC Method or LSAB Method |
Enhanced Method: Polymeric Methods |
Reagent: DAB |
Incubation Time/Temperature: 1-3 minutes/room temperature |
Reagent: Mayer's Hematoxylin |
Staining Time: 30 seconds |
Staining Pattern: Nuclear |
Images: Search image |
Tissue Type: Cells or tissues with incorporated BrdU |
Fixation: Formalin-fixed paraffin sections, or acetone fixed frozen sections |
Positive Control: Cells or tissues with incorporated BrdU |
Negative Control: Omit primary antibody, isotype control, absorption control |
Blocking: 2-5% normal serum to reduce unspecific background staining; 0.5-3% H2O2 to block endogenous peroxidase activity; avidin/biotin to block endogenous biotin activity if necessary |
Denature DNA by incubating sections in 2N HCl for 30 minutes at 37 °C, and neutralize the acid by immersing sections in 0.1M borate buffer for 2x5 min.
2N
HCl:
10N HCl --------------------------- 20 ml
Distilled water -------------------- 80 ml
Mix well.
0.1M Borate
Buffer, pH 8.5:
Sodium borate (MW 381.4) ----- 3.8 g
Distilled water -------------------- 100 ml |
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