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Polyclonal antibodies against cyclin d1

Manufactured by Santa Cruz Biotechnology
Sourced in United States

Polyclonal antibodies against cyclin D1 are a type of laboratory reagent produced by Santa Cruz Biotechnology. These antibodies are designed to recognize and bind to the cyclin D1 protein, which is involved in cell cycle regulation. The primary function of these polyclonal antibodies is to serve as a tool for researchers to detect and study the expression and localization of cyclin D1 in various biological samples.

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4 protocols using polyclonal antibodies against cyclin d1

1

Hydrangenol Inhibits Angiogenesis Signaling

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Hydrangenol was purchased from CoreSciences Co. (#BBP01679, purity 98.5%, Seoul, Korea). Human recombinant VEGF was obtained from R&D Systems (Minneapolis, MN, USA). Antibodies against ERK1/2, AKT, eNOS, VEGFR-2, phospho-ERK1/2, phospho-AKT, phospho-eNOS, and phospho-VEGFR-2 were purchased from Cell Signaling Technology Inc. (Danvers, MA, USA). Polyclonal antibodies against cyclin D1, cyclin E, CDK2, CDK4, p21WAF1, p27KIP1, p53, and GAPDH were purchased from Santa Cruz Biotechnology Inc. (Santa Cruz, CA, USA). Polyclonal antibody against MMP-2 was purchased from Chemicon (Temecula, CA, USA).
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2

Nanomaterial-Mediated Signaling Pathway Analysis

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Au@Pt-NSs were purchased from NanoSeedz™ (Hong Kong, China). The Pt:Au ratio was 1:4.19 Polyclonal antibodies against extracellular signal-regulated kinase (ERK), phospho-ERK, p38 MAPK, phospho-p38 MAPK, JNK, phospho-JNK, AKT, and phospho-AKT were obtained from Cell Signaling Technology, Inc. (Danvers, MA, USA). Polyclonal antibodies against cyclin D1, cyclin E, CDK2, CDK4, p53, p21WAF1, p27KIP1, and GAPDH were obtained from Santa Cruz Biotechnology Inc. (Dallas, TX, USA). The nuclear extract kit and the electrophoretic mobility shift assay (EMSA) gel shift kit were obtained from Panomics (Fremont, CA, USA).
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3

Immunoblotting Analysis of Cellular Signaling

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Polyclonal antibodies specific to extracellular signal regulated kinase (ERK), phospho-ERK, p38MAPK, phospho-p38MAPK, c-Jun N-terminal kinase (JNK), phospho-JNK, AKT, and phospho-AKT were obtained from Cell Signaling (Danvers, MA, USA). U0126, SP600125, SB203580, and LY294002 were obtained from Calbiochem (San Diego, CA, USA). Polyclonal antibodies against cyclin D1, cyclin E, CDK2, CDK4, p53, p21WAF1, p27KIP1, and GAPDH were obtained from Santa Cruz Biotechnology Inc. (Santa Cruz, CA, USA). Polyclonal antibodies specific to FAS, B-cell lymphoma 2 (Bcl-2), Bcl-2-associated X protein (Bax), X-linked inhibitor of apoptosis protein (XIAP), poly(ADP-ribose) polymerase-1 (PARP-1), caspase-3, caspase-6, caspase-7, caspase-8, caspase-9, and actin were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA) and Cell Signaling (Danvers, MA, USA). Polyclonal antibodies to phospho-endothelial nitric oxide synthase (eNOS) (S1177) and eNOS were obtained from Cell Signaling (Danvers, MA, USA). Human recombinant VEGF was purchased from Research and Diagnostic Systems, Inc. (Minneapolis, MN, USA).
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4

Molecular Markers in Bladder Cancer

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Antibodies for ERK, phospho-ERK, p38, phospho-p38, JNK, and phospho-JNK were purchased from Cell Signaling Technology (Danvers, MA, uSA). Polyclonal antibodies against cyclin D1, cyclin E, CDK2, CDK6, p53, p21 CIP1/WAF1 , p27 KIP1 , GAPDH, Ets-1, Sp-1, ATF-2, and CREB were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, uSA). The anti-MMP-2 antibody was obtained from Chemicon international (Billerica, Ma, uSa). mir-106a (5'-AAAAGuGCuuACAG uGCAGGuAG-3') and mir-106a inhibitor were obtained from Genolution (Seoul, Korea).
Cell cultures. Human bladder carcinoma cell lines (EJ, 5637, and T24) were purchased from the American Type Culture Collection (aTCC, Manassas, Va, uSa). Cells were cultured in Dulbecco's modified Eagle's medium (DMEM) supplemented with 10% fetal calf serum, l-glutamine, and antibiotics (Biological Industries, Beit Haemek, Israel) at 37˚C in a 5% CO 2 humidified incubator. Normal human urothelial cells (HuCs) were purchased from ScienCell Research Laboratories (Carlsbad, CA, uSA). The cells were grown in the medium specific for HuCs with supplements according to the manufacturer's protocol.
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