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1 d with Vector very intense purple (VIP) as a chromogen.
2 R or MOR using diaminobenzidine (DAB) as the chromogen.
3  utilizing tetramethylbenzidine (TMB) as the chromogen.
4 n sections by sequentially using a different chromogen.
5 ocytochemistry using diaminobenzidine as the chromogen.
6 en and Ki67 with brown 3,3'-diaminobenzidine chromogen.
7 oating sections with diaminobenzidine as the chromogen.
8 ection of neutral oligosaccharides by simple chromogens.
9 the asymmetry at C-2 during formation of the chromogens.
10 gent, indicating that they were Morgan-Elson chromogens.
11 BDA immunohistochemistry using two different chromogens.
12    To address these challenges, we introduce ChromoGen, a generative model based on state-of-the-art
13 al1-R expression was quantified by automated chromogen analysis.
14  and double immunostain using HMB45 with red chromogen and Ki67 with brown 3,3'-diaminobenzidine chro
15  or heterogeneity using the diaminobenzidine chromogen and QIF was the main outcome measure selected
16 ds for modification of these antibodies with chromogens and fluorophores.
17 phenoxazin-3-one and 7-aminophenoxazin-3-one chromogens and their corresponding beta-alanine derivati
18 tion epitopes; use of secondary reagents and chromogens; and differences in clinical end points.
19 rs in multivariate analyses both by standard chromogen detection with pathologist scoring of whole ti
20 ar base in combination with peroxidase and a chromogen did not support the growth of all of the strai
21     The concentrations of these highly polar chromogens differ from lot to lot and act as "inhibitors
22                                   Therefore, ChromoGen enables the systematic investigation of single
23       Dehydration of GlcNAc-6P by NagS to 6P-chromogen I is an unprecedented reaction in central meta
24                                           6P-chromogen I is metabolized into a structural analogue of
25 rt transplant recipients by a combination of chromogen in situ hybridization using probes specific fo
26                     A commercially available chromogen is added to the plasma sample.
27 ct was visualized with 3,3'-diaminobenzidine Chromogen Kit and lightly counterstained with Mayer's he
28 les a better understanding of the decoration chromogens nature and, thus, to determine the color pale
29 e present method, no preconcentration steps, chromogens, or complexing ligands are needed.
30 n (Cht) (a protease) and a cleavable peptide-chromogen (pro-drug) covalently incorporated into a hydr
31 ntifies and exports core images and analyses chromogen staining in a simple graphical user interface.
32 ne nasal samples and included Staphylococcus chromogenes, Staphylococcus hyicus, Aeromonas caviae, Ps
33 y CoNS strains, especially in Staphylococcus chromogenes strains.
34                                    Moreover, ChromoGen successfully transfers to cell types excluded
35 S. aureus on the basis of the utilization of chromogens that result in denim blue colonies, thus elim
36  were processed sequentially using different chromogens to visualize all three tracers in the same se
37            Loading-Release Efficiency of the chromogen was shown to exhibit a positive relation to in
38 -Ala-Ala-Pro-Phe p-nitroanilide, a cleavable chromogen, were conjugated to primary amines of a hydrat
39 re visualized by using diaminobenzidine as a chromogen, whereas CAMK(+) or PV(+) neurons were visuali
40 y ascorbic acid to provide a blue molybdenum chromogen with an absorbance maximum at 700 nm.
41                      Tetramethylbenzidine, a chromogen with strong intrinsic signal amplification of
42 and subsequent condensation of the resulting chromogens with p-dimethylaminobenzaldehyde (Ehrlich's r
43  for histiocytes, each tagged with different chromogens, yellow for pigment epithelium and purple for