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3 protocols using sec31

1

Immunofluorescence Staining of Fibroblasts

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Normal human fibroblasts or RDEB fibroblasts were plated on coverslips (Thomas Scientific, 6661-K40) in 6-well plates (Thermo Scientific, Catlog No. 140675) at 0.5 × 105 cell/well. After 48 hours, cells were fixed by 4% paraformaldehyde and blocked by 3% fetal bovine serum in 0.1% Triton X-100 for half hour at room temperature. Primary antibodies used were Collagen VII (Sigma Prestige, HPA042420, Rabbit, 1:50 dilution), Thrombospondin-1 (Santa Cruz, sc-59887, mouse, 1:50 dilution), SEC23 (Abcam, ab99552, goat, 1:100 dilution), SEC31 (Santa Cruz, sc-376587, mouse, 1:50 dilution), pSMAD3 S423/S425(Rockland, 600-401-919, Rabbit, 1:50 dilution), Calreticulin (Life Span Bioscience, LS-B5223-125, Sheep, 1:50 dilution) and Collagen I (SouthernBiotech, 1310-01, goat, 1:50). Cells with primary antibodies were incubated for 2 hours at room temperature. Secondary antibodies, Alexa Fluor 594 goat anti-rabbit (1:800) (Invitrogen, Eugene, OR), Alexa Fluor 488 goat anti-mouse (1:250) (Invitrogen, Eugene, OR), Alexa Fluor 647 donkey anti-goat (Invitrogen, Eugene, OR) and Alexa Fluor 488 donkey anti-sheep (1:250) (Invitrogen, Eugene, OR), were applied for 1 hour at room temperature. Coverslips were mounted on the slides with DAPI Fluoromount-G (SouthernBiotech, #0100-20) and analyzed by confocal microscopy (Nikon A1R Microscope).
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2

Immunofluorescence Staining of Fibroblasts

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Normal human fibroblasts or RDEB fibroblasts were plated on coverslips (Thomas Scientific, 6661-K40) in 6-well plates (Thermo Scientific, Catlog No. 140675) at 0.5 × 105 cell/well. After 48 hours, cells were fixed by 4% paraformaldehyde and blocked by 3% fetal bovine serum in 0.1% Triton X-100 for half hour at room temperature. Primary antibodies used were Collagen VII (Sigma Prestige, HPA042420, Rabbit, 1:50 dilution), Thrombospondin-1 (Santa Cruz, sc-59887, mouse, 1:50 dilution), SEC23 (Abcam, ab99552, goat, 1:100 dilution), SEC31 (Santa Cruz, sc-376587, mouse, 1:50 dilution), pSMAD3 S423/S425(Rockland, 600-401-919, Rabbit, 1:50 dilution), Calreticulin (Life Span Bioscience, LS-B5223-125, Sheep, 1:50 dilution) and Collagen I (SouthernBiotech, 1310-01, goat, 1:50). Cells with primary antibodies were incubated for 2 hours at room temperature. Secondary antibodies, Alexa Fluor 594 goat anti-rabbit (1:800) (Invitrogen, Eugene, OR), Alexa Fluor 488 goat anti-mouse (1:250) (Invitrogen, Eugene, OR), Alexa Fluor 647 donkey anti-goat (Invitrogen, Eugene, OR) and Alexa Fluor 488 donkey anti-sheep (1:250) (Invitrogen, Eugene, OR), were applied for 1 hour at room temperature. Coverslips were mounted on the slides with DAPI Fluoromount-G (SouthernBiotech, #0100-20) and analyzed by confocal microscopy (Nikon A1R Microscope).
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3

Antibody Validation for Protein Analysis

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The following antibodies were used: KLHL12 (Cell Signaling, 9406, mouse monoclonal), KLHL12 (Novus, NB120-14233, chicken polyclonal), SEC31 (BD, 612350, mouse monoclonal), SEC31 (Santa Cruz, sc-376587, mouse monoclonal), PEF1/peflin (Abcam, ab137127, rabbit monoclonal), ALG2/PDCD6 (Proteintech, 12303-1-AP, rabbit polyclonal), CUL3 (Bethyl, A301-109A, rabbit polyclonal), Lunapark (Abcam, ab121416, rabbit polyclonal), pro-collagen I (QED, 42024, mouse monoclonal), GM130 (Abcam, ab52649 rabbit monoclonal) HA (Cell Signaling, C29F4, rabbit monoclonal), FLAG (Sigma, F7425, rabbit polyclonal,), b-actin (MP Biomedicals, clone 4, mouse monoclonal), GAPDH (Cell Signaling 14C10, rabbit monoclonal), a-tubulin (Calbiochem, DM1A, mouse monoclonal). SEC13 rabbit polyclonal antibody was a gift from Randy Schekman at University of California Berkeley/HHMI. Goatanti-Mouse Alexa488 and Goat-anti-Rabbit Alexa568 (Invitrogen), Donkey-anti-Chicken IgY Fluorescien (Jackson Immunoresearch), HRP Goat-anti-Mouse IgG light-chain specific (Jackson Immunoresearch), HRP Goat-anti-Mouse IgG (Sigma), and HRP Goat-anti-Rabbit IgG (Sigma) were used as secondary antibodies.
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