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2 protocols using rabbit anti ndrg1

1

Western Blot Analysis of Cellular Proteins

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Standard Western blots were undertaken using RIPA (radioimmunoprecipitation assay) lysates as previously described [16 (link)]. A total of 10–20 ug of lysate was resolved via SDS-PAGE. Primary antibodies were as follows: anti-vinculin (1:5000) (Cat#4650, Cell Signalling Technology, Danvers, MA, USA), mouse anti-β-actin (1:5000) (Cat#sc-69879, Santa Cruz Biotechnology, Dallas, TX, USA), rabbit anti-TGM2 (1:1000) (Cat#ab2386, Abcam, Cambridge, UK), rabbit anti-FTL (Cat#ab69090, Abcam, Cambridge, UK), rabbit anti-ANXA6 (Cat#31026, Abcam, Cambridge, UK), mouse anti-MVP (Cat#ab97311, Abcam, Cambridge, UK), rabbit anti-NDRG1 (Cat#5196S, Cell Signalling Technology, Danvers, MA, USA), and rabbit anti-SOD2 (Cat#13194S, Cell Signalling Technology, Danvers, MA, USA). HRP-conjugated goat anti-mouse (Cat#1706516, Bio-Rad, Hercules, CA, USA) and goat anti-rabbit (Cat#1706515, Bio-Rad, Hercules, CA, USA) secondary antibodies were used at 1:5000 and 1:3000, respectively.
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2

Comprehensive Antibody Panel for Hypoxia Signaling

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The primary antibodies used were: mouse anti-HIF1α (BD Biosciences), rabbit anti-HIF1α (D2U3T), rabbit anti-NDRG1 (D8G9), rabbit anti-BNIP3 (D7U1T), rabbit anti-ATF4 (D4B8), mouse anti-LAMP1 (D4O1S) (Cell-signalling technology), rabbit anti-ERK2 (C14), mouse anti-GAPDH (6C5), goat anti- LDHA (N14) (Santa Cruz Biotechnologies), mouse anti-MITF (C5) (Millipore), mouse- anti-MITF (D5) (Dako), rabbit anti-MITF (HPA003259), rabbit anti-SDHB (HPA002868) (Cambridge Biosciences). rabbit anti-HIF1α and anti-HIF2α used in ChIP-seq experiments were provided by the Ratcliffe lab, rabbit anti-HIF1β (Novus Biologicals), mouse anti-FLAG (M2) (Sigma) and mouse anti-HA (12CA5) (Roche). Alexa Fluor-conjugated secondary antibodies were obtained from Invitrogen.
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