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Flt3 s 18 antibody

Manufactured by Santa Cruz Biotechnology

The FLT3 S-18 antibody is a laboratory reagent used for the detection and analysis of the FLT3 protein in biological samples. FLT3 is a receptor tyrosine kinase that plays a role in cell signaling and proliferation. This antibody can be used in various immunoassay techniques, such as Western blotting, to identify and quantify the expression of FLT3 in cell lines or tissue samples.

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2 protocols using flt3 s 18 antibody

1

Preparation and Characterization of FLT3 Inhibitor Compounds

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AGP purified from human or bovine plasma (Sigma) was resuspended in unsupplemented RPMI1640 (Gibco) at 10 mg/mL for working stocks. Recombinant human serum albumin (Sigma) was resuspended in RPMI1640 at 100 mg/mL. Lyophilized bovine plasma (Sigma) was reconstituted in sterile PBS (Gibco). TTT-3002 was a generous gift of TauTaTis, Inc. Lestaurtinib, midostaurin, sorafenib, and quizartinib were purchased from LC Laboratories. Each FLT3 TKI was dissolved at 10 mmol/L in 100% sterile-filtered dimethylsulfoxide (DMSO, Sigma). Mifepristone (Sigma) was dissolved at 100 mmol/L in 100% DMSO. Trihexyphenidyl hydrochloride (Selleckchem) was dissolved at 100 mmol/L in methanol. For cell-based assays, working stocks of 10 μmol/L were prepared for each drug in RPMI1640 supplemented with 0.1% DMSO and 0.2% BSA. For spectrophotometric studies, working stocks of 10 μmol/L were prepared using PBS without sera or albumin. ANS (Sigma) was dissolved in DMSO at 200 mmol/L and then diluted to 400 μmol/L with PBS (0.2% DMSO, final). Western blot analysis was performed using the FLT3 S-18 antibody (Santa Cruz Biotechnology) and for other proteins as indicated (Cell Signaling Technology).
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2

Characterization of FLT3 Inhibitor Interactions

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AGP purified from human or bovine plasma (Sigma) was resuspended in unsupplemented RPMI 1640 (Gibco) at 10 mg/mL for working stocks. Recombinant human serum albumin (Sigma) was resuspended in RPMI 1640 at 100 mg/mL. Lyophilized bovine plasma (Sigma) was reconstituted in sterile PBS (Gibco). TTT-3002 was a generous gift of TauTaTis, Inc. (San Diego, CA). Lestaurtinib, midostaurin, sorafenib and quizartinib were purchased from LC Laboratories. Each FLT3 TKI was dissolved at 10 mM in 100% sterile-filtered dimethylsulfoxide (DMSO, Sigma). Mifepristone (Sigma) was dissolved at 100 mM in 100% DMSO. Trihexyphenidyl hydrochloride (Selleckchem) was dissolved at 100 mM in methanol. For cell-based assays, working stocks of 10 μM were prepared for each drug in RPMI 1640 supplemented with 0.1% DMSO and 0.2% bovine serum albumin. For spectrophotometric studies, working stocks of 10 μM were prepared using PBS without sera or albumin. 8-anilinonaphthalene1-sulfonic acid (ANS, Sigma) was dissolved in DMSO at 200 mM, and then diluted to 400 μM with PBS (0.2% DMSO, final). Western analysis was performed using the FLT3 S-18 antibody (Santa Cruz), and for other proteins as indicated (Cell Signaling Technology).
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