- NeuN Rabbit mAb (A19086)
The multiplex IHC analysis on paraffin-embedded Mouse brain tissue using the following specific primary antibodies and tyramide signal amplification (TSA) reagents (RK05903) : NeuN Rabbit mAb (A19086, 1:2000) with TSA-TYR-520 (Green), GFAP Rabbit mAb (A19058, 1:500) with TSA-TYR-570 (Red), and TMEM119 Rabbit mAb (A27143, 1:600) with TSA-TYR-690 (Yellow). DAPI (Blue) was used for nuclear staining. Prior to multiplex IHC staining, high-pressure antigen retrieval was performed using 0.01M citrate buffer at pH 6.0. The analysis was completed using a 20x objective lens.
- NeuN Rabbit mAb (A19086)
The multiplex IHC analysis on paraffin-embedded Rat brain tissue using the following specific primary antibodies and tyramide signal amplification (TSA) reagents (RK05903) : NeuN Rabbit mAb (A19086, 1:2000) with TSA-TYR-520 (Green), GFAP Rabbit mAb (A19058, 1:500) with TSA-TYR-570 (Red), and TMEM119 Rabbit mAb (A27143, 1:600) with TSA-TYR-690 (Yellow). DAPI (Blue) was used for nuclear staining. Prior to multiplex IHC staining, high-pressure antigen retrieval was performed using 0.01M citrate buffer at pH 6.0. The analysis was completed using a 20x objective lens.
Western blot - NeuN Rabbit mAb (A19086)
Western blot analysis of various lysates using NeuN Rabbit mAb (A19086) at1:1000 dilution.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at1:10000 dilution.
Lysates/proteins: 25μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020).
Exposure time: 10s.
Immunohistochemistry - NeuN Rabbit mAb (A19086)
Immunohistochemistry analysis of paraffin-embedded Human brain tissue using NeuN Rabbit mAb (A19086) at a dilution of 1:2000 (40x lens). High pressure antigen retrieval performed with 0.01M Tris-EDTA Buffer(pH 9.0) prior to IHC staining.
Immunohistochemistry - NeuN Rabbit mAb (A19086)
Immunohistochemistry analysis of paraffin-embedded Rat brain tissue using NeuN Rabbit mAb (A19086) at a dilution of 1:2000 (40x lens). High pressure antigen retrieval performed with 0.01M Tris-EDTA Buffer(pH 9.0) prior to IHC staining.
Immunohistochemistry - NeuN Rabbit mAb (A19086)
Immunohistochemistry analysis of paraffin-embedded Mouse brain tissue using NeuN Rabbit mAb (A19086) at a dilution of 1:2000 (40x lens). High pressure antigen retrieval performed with 0.01M Tris-EDTA Buffer(pH 9.0) prior to IHC staining.
Immunofluorescence - NeuN Rabbit mAb (A19086)
Confocal imaging of paraffin-embedded human brain tissue using NeuN Rabbit mAb (A19086, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IF staining. Objective: 40x.
Immunofluorescence - NeuN Rabbit mAb (A19086)
Confocal imaging of paraffin-embedded mouse brain tissue using NeuN Rabbit mAb (A19086, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IF staining. Objective: 40x.
Immunofluorescence - NeuN Rabbit mAb (A19086)
Confocal imaging of paraffin-embedded rat brain tissue using NeuN Rabbit mAb (A19086, dilution 1:200) followed by a further incubation with Cy3 Goat Anti-Rabbit IgG (H+L) (AS007, dilution 1:500) (Red). DAPI was used for nuclear staining (Blue). High pressure antigen retrieval performed with 0.01M Citrate Buffer (pH 6.0) prior to IF staining. Objective: 40x.