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Rabbit anti gfp

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Rabbit anti-GFP is a primary antibody that specifically binds to the Green Fluorescent Protein (GFP). It is commonly used in various applications such as immunohistochemistry, Western blotting, and flow cytometry to detect and visualize GFP-tagged proteins in various biological samples.

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4 protocols using rabbit anti gfp

1

Immunofluorescence Staining with Diverse Antibodies

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The following primary antibodies were used: chicken anti-HTP-3 (1:1000, (46 (link))), chicken anti-GFP (1:250, (Abcam)), mouse anti-GFP (1:500, (Roche)), rabbit anti-GFP (1:500, (47 (link))), mouse anti-HA (1:1000, (Clone 16B12; Covance)), rabbit anti-MSH-5 (1:10 000, (SDIX)), rabbit anti-RAD-51 (1:500, (48 (link))), rat anti-RAD-51 (1:200, (49 (link))), guinea pig anti-SUN-1 pS24 (1:700, (50 (link))), guinea pig anti-SUN-1 pS8(1:1000, (50 (link))), guinea pig anti-SYP-1 (1:200, (51 (link))). Secondary antibodies used were Alexa Fluor 405 (1:100), 488 (1:400), 555 (1:400), and 647 (1:200)-conjugated goat antibodies raised against the appropriate species (Life Technologies).
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2

Immunostaining Characterization of Proteins

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Antibodies used in this study are as follows. Goat anti-FSTL1 (ab11805; Abcam), rabbit anti-FSTL1 (Proteintech), rabbit anti-DIAPH1 (5486; Cell Signaling Technology), rabbit anti-KSRP (A302-22A; Bethyl Laboratories), mouse anti-KRT14 (clone LLO01), mouse anti-EGF (clone 10825; R&D Systems), mouse anti-TGFβ1 (Novacastra), rabbit anti-GFP (Covance), rabbit anti-cMyc (Sigma-Aldrich), and rabbit anti-Wnt7a (ab100792; Abcam). Streptavidin Alexa Fluor 555, chicken anti-goat Alexa Fluor 488, and donkey anti-rabbit/mouse Alexa Fluor 488/555 were from Molecular Probes. Rabbit anti-Arp3 (4738), phospho (9101), and total ERK antibodies (9102) were from Cell Signaling Technology. Rabbit anti-Arpin (ABT251) was purchased from Merck Millipore. Recombinant human FSTL1 (His-tagged) expressed and purified from mammalian cells was purchased from Thermo Fisher Scientific.
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3

Immunoprecipitation of Krimper Protein Complexes

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Dissected ovaries were lysed in NT2 buffer (50 mM Tris at pH 7.4, 150 mM NaCl, 1mM MgCl2, 0.05% Igepal, EDTA-free Complete Protease Inhibitor Cocktail). Lysate was incubated in the presence or absence of 100µg/mL RNAse A, cleared by centrifugation and incubated with anti-FLAG M2 beads (Sigma Aldrich) at 4°C for 90 min., follow ed by washing and elution in reducing SDS buffer. Antibodies used for Western Blots were rabbit anti-GFP (Covance), mouse anti-GFP B-2 (Santa Cruz Biotechnology) or anti-FLAG M2 (Sigma Aldrich) at 1:3,000 concentration. Anti-Krimper rabbit polyclonal antibody generously provided by Dr. T. Kai was used at a concentration of 1:20,000. A variant protocol for S2 cell co-immunoprecipitation and other details are provided in the Supplemental Experimental Procedures.
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4

Immunofluorescence Staining of Meiotic Proteins

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The following primary antibodies were used at the indicated dilutions: Chicken anti-HTP-3 (1:500) (MacQueen et al., 2005 (link)), guinea pig anti-HTP-3 (1:500) (MacQueen et al., 2005 (link)), rabbit anti-MSH-5 (1:10000) (SDI/Novus), chicken anti-GFP (1:2000) (Abcam), mouse anti-GFP (1:500) (Roche), rabbit anti-GFP (1:500) (Yokoo et al., 2012 (link)), mouse anti-HA (1:1000) (Covance), guinea pig anti-ZHP-3 (1:500) (Bhalla et al., 2008 (link)), rabbit anti-PLK-2 (Nishi et al., 2008 (link)), guinea pig anti-SYP-1 (1:200) (MacQueen et al., 2002 (link)), rat anti-RAD-51 (1:200) (Rosu et al., 2013 (link)), rabbit anti-RPA-1 (1:500) (Lee et al., 2010 (link)), mouse anti-H3K4me2 (1:2000) (Merck), rabbit anti-SYP-1 (1:2000) (MacQueen et al., 2002 (link)) and rabbit anti-SYP-2 (1:200) (Colaiacovo et al., 2003 (link)).
Secondary antibodies conjugated to Alexa dyes 405, 488, 555 or 647, obtained from Molecular Probes, were used at 1:500 dilution. In cases where antibodies raised in mouse and guinea pig were used on the same sample, we used highly cross-absorbed goat anti-mouse secondary antibodies, obtained from Biotum (conjugated to CF488, or CF555 respectively) for secondary detection of the mouse primary antibody in order to avoid cross-reaction against antibodies raised in guinea pig.
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