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Hrp conjugated anti rabbit igg

Manufactured by Vector Laboratories
Sourced in Canada

HRP-conjugated anti-rabbit IgG is a secondary antibody that binds to rabbit primary antibodies. It is labeled with horseradish peroxidase (HRP), an enzyme that can be used for signal detection in various immunoassays and immunohistochemical applications.

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3 protocols using hrp conjugated anti rabbit igg

1

Immunostaining of Astrocytes in WT and RGC-32 KO Mice

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WT and RGC-32 KO mouse astrocytes were plated on Permanox® Chamber Slide culture chambers (Nunc Inc, Rochester, NY) for 24 h, fixed in acetone for 10 min, and then air-dried. The sections were washed in PBS and then incubated with 0.3% hydrogen peroxide diluted in PBS for 10 min to quench the endogenous peroxidase. The slides were incubated with primary rabbit anti-GFAP antibody (Dako Agilent, Santa Clara, CA) overnight at 4°C and then with HRP-conjugated anti-rabbit IgG (Vector Labs) for 30 min. NovaRed (Vector Labs) was used as the chromogenic substrate.
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2

Comprehensive Antibody Panel for Studying Chromosome Segregation

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Primary antibodies used in in the present study were as follows: anti-XSMC4/XCAP-C (in-house identifier AfR8L, affinity-purified rabbit antibody), anti-XSMC2/XCAP-E (AfR9-6, affinity-purified rabbit antibody), anti-XCAP-D2 (AfR16L, affinity-purified rabbit antibody), anti-XCAP-G (AfR11-3L, affinity-purified rabbit antibody; Hirano and Mitchison, 1994 (link); Hirano et al., 1997 (link)), anti-XCAP-D3 (AfR196-2L, affinity-purified rabbit antibody), anti-XCAP-H2 (AfR201-4, affinity-purified rabbit antibody; Ono et al., 2003 (link)), anti-mSMC4 (AfR326-3L, affinity-purified rabbit antibody; Lee et al., 2011 (link)), anti-XSMC3 (AfR48-5L, affinity-purified rabbit antibody; Losada et al., 1998 (link)), anti–topo IIα (in-house identifier αC1-6, rabbit anti-serum; Hirano and Mitchison, 1993 (link)), anti-histone H3 (CMA301: MABI0301 [RRID AB_1977240]; MBL, mouse antibody), and anti-topo II (AK5: M052-3 [RRID AB_592894]; MBL, mouse antibody). Secondary antibodies used in the present study were as follows: HRP-conjugated anti-rabbit IgG (PI-1000 [RRID AB_2336198], Vector Laboratories, goat antibody), Alexa Fluor 488 anti-rabbit IgG (A-11008 [RRID AB_143165], Thermo Fisher Scientific, goat antibody), Alexa Fluor 568 anti-mouse IgG (A-10037 [RRID AB_2534013], Thermo Fisher Scientific, donkey antibody).
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3

Western Blotting with Antibody Details

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Western blot was carried out following standard procedures using antibodies listed here: mouse anti-V5 (1:5000, Invitrogen), mouse anti-HA (1:2000, Roche), chicken anti-HA (1:2000, Aves), rabbit anti-Flag (1:2000, Sigma-Aldrich), HRP-conjugated anti-mouse IgG (1:5000–1:10000, Vector), HRP-conjugated anti-chicken IgG (1:5000, Jackson Immunoresearch), HRP-conjugated anti-rabbit IgG (1:1000–1:5000, Vector), mouse dCaMKII (Cosmo CAC-TNL-001-CAM 1:1000), rabbit α-p-CaMKIIα (Thr 286) (Santa Cruz sc-12886-R 1:1000), mouse Tubulin DM1A (Abcam ab7291 1:10000).
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