vip chromagen solution Search Results


95
Vector Laboratories chromogen vip
Chromogen Vip, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/chromogen vip/product/Vector Laboratories
Average 95 stars, based on 1 article reviews
chromogen vip - by Bioz Stars, 2026-03
95/100 stars
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86
Vector Laboratories vip chromagen solution
Vip Chromagen Solution, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/vip chromagen solution/product/Vector Laboratories
Average 86 stars, based on 1 article reviews
vip chromagen solution - by Bioz Stars, 2026-03
86/100 stars
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93
Vector Laboratories vector vip substrate chromogen solution
Vector Vip Substrate Chromogen Solution, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/vector vip substrate chromogen solution/product/Vector Laboratories
Average 93 stars, based on 1 article reviews
vector vip substrate chromogen solution - by Bioz Stars, 2026-03
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86
Vector Laboratories vector vip chromogen solution
Iba1 immunostaining of free floating sections following different antigen methods. Wild type (WT) and APP/PS1 free floating 40 μm tissue sections were untreated (no treatment) or processed through single or combined antigen retrieval methods (trypsin-EDTA, 10 mM EDTA pH 6.0, formic acid, combined treatment) before immunostaining using anti-Iba1 antibody. Representative Iba1 immunostained images visualized using vector <t>VIP</t> as <t>the</t> <t>chromogen</t> taken from the temporal cortex are shown from (a) wild type (WT) no treatment control, (b) APP/PS1 no treatment control, (c) WT trypsin-EDTA antigen retrieval, (d) APP/PS1 trypsin-EDTA antigen retrieval, (e) WT 10 mM EDTA, pH 6.0 antigen retrieval, (f) APP/PS1 10 mM EDTA, pH 6.0 antigen retrieval, (g) WT formic acid antigen retrieval, (h) APP/PS1 formic acid antigen retrieval, (i) WT combined treatment antigen retrieval, and (j) APP/PS1 combined treatment antigen retrieval.
Vector Vip Chromogen Solution, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/vector vip chromogen solution/product/Vector Laboratories
Average 86 stars, based on 1 article reviews
vector vip chromogen solution - by Bioz Stars, 2026-03
86/100 stars
  Buy from Supplier

Image Search Results


Iba1 immunostaining of free floating sections following different antigen methods. Wild type (WT) and APP/PS1 free floating 40 μm tissue sections were untreated (no treatment) or processed through single or combined antigen retrieval methods (trypsin-EDTA, 10 mM EDTA pH 6.0, formic acid, combined treatment) before immunostaining using anti-Iba1 antibody. Representative Iba1 immunostained images visualized using vector VIP as the chromogen taken from the temporal cortex are shown from (a) wild type (WT) no treatment control, (b) APP/PS1 no treatment control, (c) WT trypsin-EDTA antigen retrieval, (d) APP/PS1 trypsin-EDTA antigen retrieval, (e) WT 10 mM EDTA, pH 6.0 antigen retrieval, (f) APP/PS1 10 mM EDTA, pH 6.0 antigen retrieval, (g) WT formic acid antigen retrieval, (h) APP/PS1 formic acid antigen retrieval, (i) WT combined treatment antigen retrieval, and (j) APP/PS1 combined treatment antigen retrieval.

Journal: MethodsX

Article Title: Iba1 immunoreactivity is enhanced following an antigen retrieval treatment with EDTA, pH 6.0

doi: 10.1016/j.mex.2014.10.007

Figure Lengend Snippet: Iba1 immunostaining of free floating sections following different antigen methods. Wild type (WT) and APP/PS1 free floating 40 μm tissue sections were untreated (no treatment) or processed through single or combined antigen retrieval methods (trypsin-EDTA, 10 mM EDTA pH 6.0, formic acid, combined treatment) before immunostaining using anti-Iba1 antibody. Representative Iba1 immunostained images visualized using vector VIP as the chromogen taken from the temporal cortex are shown from (a) wild type (WT) no treatment control, (b) APP/PS1 no treatment control, (c) WT trypsin-EDTA antigen retrieval, (d) APP/PS1 trypsin-EDTA antigen retrieval, (e) WT 10 mM EDTA, pH 6.0 antigen retrieval, (f) APP/PS1 10 mM EDTA, pH 6.0 antigen retrieval, (g) WT formic acid antigen retrieval, (h) APP/PS1 formic acid antigen retrieval, (i) WT combined treatment antigen retrieval, and (j) APP/PS1 combined treatment antigen retrieval.

Article Snippet: The free floating tissue or slide mounted tissue sections were rinsed four times with PBS only, then incubated for 5 min with a Vector VIP chromogen solution according to manufacturer's instructions (Vector VIP peroxidase substrate kit, Violet SK-4600, Vector Laboratories) to develop the immunostains.

Techniques: Immunostaining, Plasmid Preparation

Morphology of Iba1 immunoreactive microglia on slide mounted sections visualized after 10 mM EDTA, pH 6.0 antigen retrieval. Wild type (WT) and APP/PS1slide mounted brain sections, 10 μm, were untreated (no treatment) or processed for antigen retrieval using 10 mM EDTA, pH 6.0 before immunostaining using anti-Iba-1 antibody and visualized using vector VIP as the chromogen. Representative temporal cortex images are shown from (a) Wild type (WT) no treatment control, (b) APP/PS1 no treatment control, (c) WT 10 mM EDTA, pH 6.0 antigen retrieval, and (d) APP/PS1 10 mM EDTA, pH 6.0 antigen retrieval conditions.

Journal: MethodsX

Article Title: Iba1 immunoreactivity is enhanced following an antigen retrieval treatment with EDTA, pH 6.0

doi: 10.1016/j.mex.2014.10.007

Figure Lengend Snippet: Morphology of Iba1 immunoreactive microglia on slide mounted sections visualized after 10 mM EDTA, pH 6.0 antigen retrieval. Wild type (WT) and APP/PS1slide mounted brain sections, 10 μm, were untreated (no treatment) or processed for antigen retrieval using 10 mM EDTA, pH 6.0 before immunostaining using anti-Iba-1 antibody and visualized using vector VIP as the chromogen. Representative temporal cortex images are shown from (a) Wild type (WT) no treatment control, (b) APP/PS1 no treatment control, (c) WT 10 mM EDTA, pH 6.0 antigen retrieval, and (d) APP/PS1 10 mM EDTA, pH 6.0 antigen retrieval conditions.

Article Snippet: The free floating tissue or slide mounted tissue sections were rinsed four times with PBS only, then incubated for 5 min with a Vector VIP chromogen solution according to manufacturer's instructions (Vector VIP peroxidase substrate kit, Violet SK-4600, Vector Laboratories) to develop the immunostains.

Techniques: Immunostaining, Plasmid Preparation

Aβ immunostaining of free floating sections following different antigen retrieval methods. Wild type (WT) and APP/PS1 free floating 40 μm tissue sections were untreated (no treatment) or processed through single or combined antigen retrieval methods (trypsin-EDTA, 10 mM EDTA pH 6.0, formic acid, combined treatment) before immunostaining using anti-Aβ antibody. Representative Aβ immunostained images visualized using vector VIP as the chromogen taken from the temporal cortex are shown from (a) wild type (WT) no treatment control, (b) APP/PS1 no treatment control, (c) WT trypsin-EDTA antigen retrieval, (d) APP/PS1 trypsin-EDTA antigen retrieval, (e) WT 10 mM EDTA, pH 6.0 antigen retrieval, (f) APP/PS1 10 mM EDTA, pH 6.0 antigen retrieval, (g) WT formic acid antigen retrieval, (h) APP/PS1 formic acid antigen retrieval, (i) WT combined treatment antigen retrieval, and (j) APP/PS1 combined treatment antigen retrieval.

Journal: MethodsX

Article Title: Iba1 immunoreactivity is enhanced following an antigen retrieval treatment with EDTA, pH 6.0

doi: 10.1016/j.mex.2014.10.007

Figure Lengend Snippet: Aβ immunostaining of free floating sections following different antigen retrieval methods. Wild type (WT) and APP/PS1 free floating 40 μm tissue sections were untreated (no treatment) or processed through single or combined antigen retrieval methods (trypsin-EDTA, 10 mM EDTA pH 6.0, formic acid, combined treatment) before immunostaining using anti-Aβ antibody. Representative Aβ immunostained images visualized using vector VIP as the chromogen taken from the temporal cortex are shown from (a) wild type (WT) no treatment control, (b) APP/PS1 no treatment control, (c) WT trypsin-EDTA antigen retrieval, (d) APP/PS1 trypsin-EDTA antigen retrieval, (e) WT 10 mM EDTA, pH 6.0 antigen retrieval, (f) APP/PS1 10 mM EDTA, pH 6.0 antigen retrieval, (g) WT formic acid antigen retrieval, (h) APP/PS1 formic acid antigen retrieval, (i) WT combined treatment antigen retrieval, and (j) APP/PS1 combined treatment antigen retrieval.

Article Snippet: The free floating tissue or slide mounted tissue sections were rinsed four times with PBS only, then incubated for 5 min with a Vector VIP chromogen solution according to manufacturer's instructions (Vector VIP peroxidase substrate kit, Violet SK-4600, Vector Laboratories) to develop the immunostains.

Techniques: Immunostaining, Plasmid Preparation