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Rat anti mouse cd31 polyclonal antibody

Manufactured by BD
Sourced in United States

The Rat anti-mouse CD31 polyclonal antibody is a laboratory reagent used to detect the presence of CD31, also known as PECAM-1, in mouse biological samples. CD31 is a cell adhesion molecule expressed on the surface of endothelial cells, platelets, and some leukocytes. This antibody can be used for various research applications involving the identification and study of CD31-expressing cells.

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3 protocols using rat anti mouse cd31 polyclonal antibody

1

Luteolin and Tumor Angiogenesis Inhibition

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Materials were purchased from standard sources: luteolin from Sigma (St Louis, MO, USA); MTT from Sigma; DMEM and FBS from Gibco BRL (Waltham, MA, USA); methanol and acetic acid (HPLC grade) from Fisher Scientific  (Waltham, MA, USA); and dimethyl sulfoxide (DMSO) and acetone from KeLong Chemicals (Chengdu, China). Antibodies used include rat anti-mouse CD31 polyclonal antibody (BD Pharmingen™, Franklin Lake, NJ, USA), rabbit anti-mouse PCNA antibody (Abcam, Cambridge, UK), and rhodamine-conjugated secondary antibody (Abcam). NH2-PEG-PCL was purchased from ruixi Biological Technology Company (Xian, China).
C57 mice (6–8 weeks) and Sprague Dawley (SD) rats were purchased from the Animal Center Laboratory of Beijing HFK Bioscience Co Ltd (Beijing, People’s Republic of China). All mice were housed in a controlled temperature of 20–22°C, with a relative humidity of 50–60% and 12 hr light-dark cycles. The animals were provided with standard laboratory chow and tap water ad libitum. All animal procedures were performed following the protocol approved by the Institutional Animal Care and Treatment Committee of Sichuan University (Chengdu, People’s Republic of China) and treated humanely throughout the experimental period.
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2

Quantifying Tumor Angiogenesis and Proliferation

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The angiogenic activity and cell proliferative potential of each tumor was detected by CD31 or Ki-67 immunofluorescence staining of paraffin-embedded tumor tissue sections, described above. Briefly, frozen sections of tumor tissue from each group were fixed in acetone, washed with PBS, and then stained with a rat anti-mouse CD31 polyclonal antibody (BD PharmingenTM, USA) or rabbit anti-mouse Ki67 monoclonal antibody (Abcam, USA). Subsequently, the sections were washed with PBS twice, and were then incubated with a rhodamine-conjugated secondary antibody (Abcam, USA). The microvessel density (MVD) was determined by counting the number of microvessels per high-power field (400x magnification) in each section using a fluorescence microscope. Five high-power fields of tumor section were randomly selected and analyzed in a blind fashion by two independent investigators for this procedure. The Ki-67 labeling index (Ki-67 LI) was used to quantify the expression of Ki-67 by calculating the number of KI-67-positive cells per total number of cells.
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3

MPEG-PCL Diblock Copolymer Synthesis and Characterization

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Luteolin and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) from Sigma (USA); Dulbecco’s Modified Eagle’s Medium (DMEM) and fetal bovine serum (FBS) from Gibco BRL (USA); methanol and acetic acid (HPLC grade) from Fisher Scientific (UK); and dimethyl sulfoxide (DMSO) and acetone from KeLong Chemicals (China). Antibodies purchased include: rat anti-mouse CD31 polyclonal antibody (BD PharmingenTM, USA), rabbit anti-mouse Ki67 antibody (Abcam, USA), and rhodamine-conjugated secondary antibody (Abcam, USA).
The MPEG (molecular weight = 2000) (Sigma–Aldrich, St. Louis, MO, USA) was dried in a one-necked flask under vacuum and magnetically stirred at 105 °C for 90 min before use.
MPEG (2000)-PCL(2000) diblock copolymer with a molecular weight of 4000 was synthesized by ring opening of ε-caprolactone, which was initiated by MPEG as descripting previously [21 (link)]. Briefly, MPEG and ε-CL were introduced into a dry glass ampoule under a nitrogen atmosphere. Sn(Oct)2 was then added into the reaction vessel under mild agitation, and the reaction system was kept at 130 °C for 6 h. The purified MPEG-PCL copolymer was kept in a desiccator before further use.
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