ImmunoChemistry Technologies

303 products

ImmunoChemistry Technologies is your partner in cell viability assays, ELISA reagents, IHC reagents, and immunoassay services. With decades of protein chemistry expertise, ICT offers a wide range of products for immunoassay, cellular, and molecular diagnostics development. Our kits include fluorescent whole cell assays for intracellular apoptosis detection, autophagy, oxidative stress, caspase activity, and more. Optimize your technique with our coating and wash buffers, blockers, sample and assay diluents, stabilizers, and stop solutions. From ELISA development and plate coating, to IHC counterstains and mounting media, to antibody conjugation and purification, the team at our ISO-13485-certified facility in Davis, California is dedicated to helping you build a better assay.

Showing 121 - 144 of 303 products

ImmunoChemistry Technologies ImmunoFluoroMount™ with PPD

From $80.75

ImmunoChemistry Technologies Glycerol Fluoro Mount with PPD

From $80.75

ImmunoChemistry Technologies Glycerol Mounting Medium with DAPI and DABCO

From $97.25

ImmunoChemistry Technologies Glycerol Mounting Medium with DABCO

From $85.75

ImmunoChemistry Technologies Glycerol Mounting Medium

From $74.50

ImmunoChemistry Technologies Immuno In Situ Mount™

From $85.75

ImmunoChemistry Technologies Fluoroshield™ with DAPI & Propylgallate

From $97.25

Representative section of formalin fixed, paraffin-embedded rat brain hippocampus region showing staining of GFAP. The sections were stained with Antibodies Incorporated anti-GFAP antibody (visualized in green) (Cat No. 75-240) at 1:500 dilution. The stained sections were mounted with Antibodies Incorporated FluoroshieldTM with DAPI and DABCO mounting medium (Cat. No. AR-6505). DAPI nuclear stain (blue) shows cell nuclei. Anti-GFAP specifically stains the astrocytes in the rat brain.

Representative section of formalin fixed, paraffin-embedded rat brain showing staining of GFAP. The sections were stained with Aves Labs anti-GFAP antibody (visualized in green) (Cat. No. GFAP) at 1:500 dilution. The stained sections were mounted with Antibodies Incorporated FluoroshieldTM with DAPI and DABCO mounting medium (Cat No. AR-6505). DAPI nuclear stain (blue) shows cell nuclei. Anti-GFAP specifically stains the astrocytes in the rat brain.

ImmunoChemistry Technologies Fluoroshield™ with DAPI & DABCO

From $97.25

ImmunoChemistry Technologies Organo / Limonene Mount™

From $80.50

ImmunoChemistry Technologies ImmunoHistoMount™

From $85.75

ImmunoChemistry Technologies Fluoroshield™ with PI

From $97.25

Immunofluorescent staining of HeLa cells using 2 µg/mL Aves Labs chicken anti-Giantin (GOLGB1) (Cat. No. GOLGB1-0100) antibody (green). Actin filaments were stained using Phalloidin (red). DAPI nuclear stain (blue) shows cell nuclei. The cells were mounted with Antibodies Incorporated Fluoroshield with DAPI and DABCO mounting medium (Cat. No. AR-6505). Anti-Giantin specifically stains the Golgi apparatus in HeLa cells.

Immunofluorescent staining of HeLa cells using 2 µg/mL chicken anti-Calnexin (CANX) antibody (green). DAPI nuclear stain (blue) shows cell nuclei. The cells were mounted with Antibodies Incorporated Fluoroshield with DAPI mounting medium (Cat No. AR-6501). Anti-Calnexin specifically stains the Endoplasmic Reticulum in HeLa cells.

ImmunoChemistry Technologies Fluoroshield™ with DAPI

From $97.25

Distribution of α2δ-1 subunit in spinal dorsal horn. The spinal dorsal horn sections of CV mice were stained with anti-α2δ-1 antibody (green). Scale bar = 200 µm. Solid line represents the gray matter border, dotted line represents the superficial layer. Sections mounted with Fluoroshield medium (Cat no AR-6500, ImmunoBioScience Corp). Image from publication CC-BY-4.0. PMID: 38989140

ImmunoChemistry Technologies Fluoroshield™

From $85.75

Figure 1. Assay principle: a non‐fluorescent detection reagent is oxidized in the presence of hydrogen peroxide and MPO to produce its fluorescent analog.

Figure 2. A MPO standard curve was prepared and run, as described in the protocol, in the absence (A) or presence (B) of 20 mM catalase inhibitor. MPO standard and reaction mix were added to a 96-well black plate and incubated at room temperature in the dark for 30 minutes. The wells were read using Ex: 530nm and Em: 590nm. There is an approximately 50% reduction in signal in the presence of 20mM catalase inhibitor (note the different scales on the x-axis).

ImmunoChemistry Technologies Myeloperoxidase Detection Kit

$506

Figure 2. Typical standard curve. A new curve must be generated each time the assay is run.

ImmunoChemistry Technologies Fluorescent Sarcosine Detection Kit

$357

Figure 2. Bovine serum Semicarbazide-sensitive amine oxidase was serially diluted in 1X Reaction buffer. The serially diluted samples were run as described in the protocol. The samples were read after a 3 hours incubation period. Excitation: 530 nm and emission: 590 nm.

ImmunoChemistry Technologies Fluorescent Semicarbazide-Sensitive Amine Oxidase Detection Kit

$475

Figure 2. Phosphate standard curve was generated using fluorometric detection: excitation 535 nm and emission 585 nm. Incubation time = 60 minutes at 37°C. Standard curve range 1.5625 μM to 100μM. Graph was plotted using 4PL non-linear regression.

ImmunoChemistry Technologies Fluorescent Phosphate Detection Kit

$269

ImmunoChemistry Technologies Fluorescent Monoamine Oxidase Detection Kit

$289

ImmunoChemistry Technologies Fluorescent Lactate Detection Kit

$429

Figure 1. Staurosporine induced Jurkat cell viability assay. Titrated doses of staurosporine were added into seeded Jurkat cells (10,000 cells/well) in 96-well black opaque tissue culture plates and incubated at 37°C, 10% CO2 for 24h. Dye reagent (1/10 volume) was added into the cultured cells and incubated for 3h and fluorescence was detected at Ex: 530 nm and Em: 590 nm.

Figure 2. PBMC proliferation in response to mitogen Concanavalin A (Con-A) stimulation measured using Fluorescent Cell Proliferation Assay. PBMC at 15,000 cells were cultured for 3 days in the presence of titrated amounts of Con A and tested for proliferation using the Fluorescent Cell Proliferation Assay. Dye reagent (1/10 volume) was added to the cultured cells and incubated at 37°C for 2h. Fluorescence was detected at Ex: 530 nm and Em: 590 nm.

ImmunoChemistry Technologies Fluorescent Cell Proliferation Assay

From $114

Figure 2. The reaction contained 20mM hydrogen peroxide (final) per well and the indicated amounts of catalase. The reaction was incubated for 30 minutes at room temperature. Reaction cocktail was added to each well and the reaction incubated for another 10 minutes in the dark at room temperature. Fluorescence was measured at excitation 530nm and emission 590nm. The graphs show the net fluorescence change: Negative Control fluorescence (no catalase) minus Sample (catalase) fluorescence.

ImmunoChemistry Technologies Fluoro Catalase Activity Detection Kit by Cell Technology

$341

ImmunoChemistry Technologies Fluorescent ATP Detection Kit

From $393

ImmunoChemistry Technologies Fluorescent ADP Detection Kit

From $393

ImmunoChemistry Technologies Fluoro AChE - a fluorescence assay for monitoring and detecting acetylcholinesterase activity in samples

From $486

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