The largest database of trusted experimental protocols

4 protocols using cd31 sc 1506

1

Immunohistochemical Analysis of PCNA, CD31, and TUNEL

Check if the same lab product or an alternative is used in the 5 most similar protocols
Slides were re-hydrated in PBS for 15 min, and the endogenous peroxidase was then inhibited using 3% H2O2/methanol for 10 min at room temperature. For blocking, 5% non-fat milk/PBS was used for 30 min at room temperature. Slides were incubated with either anti-human PCNA (sc-56, Santa Cruz Biotechnology), CD31 (sc-1506, Santa Cruz Biotechnology) antibodies or a TUNEL reagent (R&D Systems) for 16 hrs at 4 °C. The peroxidase-conjugated secondary antibody was incubated for 1 hr at room temperature and developed by immersing slides in 0.06% 3,3’-diaminobenzidine tetrahydrochloride, followed by counterstaining with Gill’s hematoxylin.
+ Open protocol
+ Expand
2

Angiogenesis Assay Protocol with 3-HBA

Check if the same lab product or an alternative is used in the 5 most similar protocols
3-Hydroxylbenzaldehyde (3-HBA) was purchased from Sigma Aldrich (St. Louis, MO, USA), dissolved in water, and filtered using a 0.2-μm pore cellulose acetate syringe filter (16534-K; Sartorious, Goettingen, Germany). TNF-α and rat PDGF-BB were purchased from R&D Systems (Minneapolis, MN, USA). Heparin and normal saline were purchased from JW Pharmaceutical (Seoul, Korea). Antibodies for Western blot analysis against VCAM-1 (sc-8304), ICAM-1 (sc-7891), MMP-2 (sc-10736), and CD31 (sc-1506) were purchased from Santa Cruz (Delaware, CA, USA). Phospho-AKT (#9271S), AKT (#9272S), phospho-MAPK (#9106S), NFκB (#4767), and phospho-NFκB (#3033S) were purchased from Cell Signaling Technology (Danvers, MA, USA). Cultrex BME Matrigel (3431-005-01) was purchased from Trevigen (Gaithersburg, MD, USA) for use in the sprout ring assay. MTS assay kit (G3580) was purchased from Promega (Madison, WI, USA). Propidium iodide (PI) was purchased from Sigma Aldrich for use in cell cycle assay. Bromodeoxyuridine (BrdU) incorporation assay kit was purchased from Roche (Basel, Switzerland) for use in cell proliferation ELISA assay.
+ Open protocol
+ Expand
3

Immunostaining of Tumor Angiogenesis and Proliferation

Check if the same lab product or an alternative is used in the 5 most similar protocols
Formalin fixed, paraffin-embedded tumor sections were immunostained using the following reagents: For microvessel density (MVD; CD34+ and CD31+ vessels), 1:150 CD34 (LS-C47878; LifeSpan Biosciences), 1:100 CD31 (sc-1506; Santa Cruz Biotechnology), Cy3- and Alexa488-conjugated secondary antibodies (Jackson Immunoresearch) and DAPI (Invitrogen); for cell proliferation (human Ki-67), 1:1,000 Ki-67 antibody (VP-K451; Vector Laboratories), LSAB+ and DAB+ kits (Dako), and hematoxylin (Surgipath). Approximately 20 images/section were obtained (n = 4–9/group) at ×100 (Ki-67) or ×200 (MVD). CD34+ or CD31+ microvessel counts and Ki-67 stain were normalized to nuclear stain using ImageJ (v.1.46r) software.
+ Open protocol
+ Expand
4

Immunofluorescence Staining of Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
Cells were seeded on glass slide and cultured in corresponding media until achieved 80% confluency. After washing with PBS, cells or frozen sections were fixed with 4% paraformaldehyde (PFA) (Sigma-Aldrich) for 15 minutes and then permeabilized with 0.1% Triton X-100 (Sigma-Aldrich) for another 15 minutes. Samples were blocked with 5% appropriate serum/1 × PBS at 37 °C for 30 minutes followed by incubation with primary antibodies at 37 °C for 1 hour: CD34 (sc7324, Santa Cruz, 1:50); CD31 (sc1506, Santa Cruz, 1:50); eNOS (610297, BD Biosciences, 1:50); CD144 (sc6458, Santa Cruz, 1:50); KDR (ab9530, Abcam, 1:100); human specific CD31 (ab32457, Abcam, 1:100); HES5 (Ab5708, Millipore, 1:50); vWF (ab6994, Abcam, 1:100); VCAM-1 (sc-13160, Santa Cruz, 1:50); ICAM-1 (MA5-13021, ThermoFisher, 1:50). After washing with PBS, samples were incubated with the appropriate Alexa Fluor-conjugated secondary antibodies (Invitrogen, 1:500) for 45 minutes at 37 °C. Samples were washed with PBS and then DAPI (Sigma Aldrich) was applied for 3 minutes. The slides were mounted with Fluorescent Mounting Media (Dako) and images were acquired by Olympus IX81 microscope equipped with TRITC, FITC and DAPI filters.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!