conjugated

Thiazole Orange is a dye that can be used for reticulocyte analysis.

FITC-dextran (MW 4000) is a fluorescein isothiocyanate (FITC) Dextran fluorescent probe (Ex=495 nm; Em=525 nm). FITC-Dextran (MW 4000) can be used as a marker to reveal cell damage caused by heat shock and to study the early and late stages of apoptosis. FITC-Dextran (MW 4000) can also be used for cell permeability studies, such as the determination of blood-brain barrier permeability and the degree of blood-brain barrier disruption.

Ac4ManNDAz is a cell-permeable photocrosslinking probe that is a precursor to photocrosslinked sialic acid, which attaches to cell surface α2-6-conjugated sialic acid and produces photocrosslinking via sialic acid.

Phthalocyanine (29H,31H-Phthalocyanine) is an important multifunctional dye. It is a planar macrocyclic conjugated system composed of four isoindole units. It can form complexes with a variety of metals and can be used to synthesize new organic materials.

5-Aminofluorescein (5-AF) (5-AF) is a covalently-bound fluorescence marker conjugated with human serum albumin. It exhibits an excitation wavelength of 490 nm and an emission wavelength of 515 nm.

Alkyne-tagged dopamine is an endogenous neurotransmitter dopamine derivative designed for click chemistry, already conjugated with a fluorescent group, and used in research to characterize dopamine dynamics.

BQ7876 is a probe that targets prostate-specific membrane antigen (PSMA) and contains a DOTA chelator. After radiolabeling with radionuclides (177Lu), BQ7876 specifically binds to PSMA, serving both in radionuclide imaging and tumor cell destruction. It shows potential for research in the field of metastatic castration-resistant prostate cancer (mCRPC). BQ7876 can also be utilized in the synthesis research of radionuclide conjugated drugs (RDC).

Wheat germ agglutinin-AF350 (WGA-AF350) is a plant lectin conjugated with the fluorescent dye AF350, utilized for identifying carbohydrate chains. It serves as a tool for assessing abnormal glycosylation levels in vivo. The specific glycosylation detection sites of Wheat germ agglutinin are bis-GlcNAc and SA.

Wheat germ agglutinin-AF647 (WGA-AF647) is a plant lectin conjugated with the fluorescent dye AF647, designed for identifying carbohydrate chains. This compound is utilized to evaluate abnormal glycosylation levels in vivo. The specific glycosylation detection sites for wheat germ agglutinin include bis-GlcNAc and SA.

Wheat germ agglutinin-AF750 (WGA-AF750) is a plant lectin conjugated with the fluorescent dye AF750, used to identify carbohydrate chains. It serves in evaluating aberrant glycosylation levels in vivo. The specific glycosylation detection sites for wheat germ agglutinin are bis-GlcNAc, SA.

TRITC-lysine-dextran, 70kDa, is a dextran conjugated with lysine and contains the fluorescent group TRITC. Lysine-dextran exhibits greater glutamic acid-plasminogen binding capacity compared to dextran alone.

FITC-lysine-dextran, 500kDa, is a dextran conjugated with lysine and incorporates the fluorescent group FITC. Compared to dextran alone, lysine-dextran exhibits enhanced binding capacity for glutamic-plasminogen.

TRITC-lysine-dextran, 500kDa, is a dextran polymer conjugated with lysine and incorporates the fluorescent group TRITC. Compared to dextran alone, lysine-dextran exhibits a greater capacity for glutamic acid-plasminogen binding.

FITC-lysine-dextran, 4kDa, is a dextran compound conjugated with lysine and incorporates the fluorescent group FITC. Compared to dextran alone, lysine-dextran exhibits enhanced glutamic acid-plasminogen binding capacity.

FITC-lysine-dextran, 10kDa, is a dextran compound conjugated with lysine and contains the fluorescent group FITC. Lysine-dextran exhibits an enhanced ability to bind glutamic acid-plasminogen compared to dextran alone.

Wheat germ agglutinin-AF532 (WGA-AF532) is a plant lectin conjugated with the fluorescent dye AF532, used for identifying carbohydrate chains. This compound can assess abnormal glycosylation levels in vivo. The specific glycosylation detection sites of Wheat germ agglutinin are bis-GlcNAc, SA.

FITC-lysine-dextran (70 kDa) is a dextran conjugated with lysine and contains the fluorescent moiety FITC. Lysine-dextran demonstrates enhanced glutamic acid-plasminogen binding capacity compared to dextran alone.

TRITC-lysine-dextran, 4kDa is a dextran that is conjugated with lysine and contains the fluorescent group TRITC. Compared to dextran alone, lysine-dextran exhibits enhanced binding capacity to glutamic acid-plasminogen.

Wheat germ agglutinin-AF488 (WGA-AF488) is a plant lectin conjugated with the fluorescent dye AF488, designed for identifying carbohydrate chains. WGA-AF488 is applicable in assessing abnormal glycosylation levels in vivo. The specific glycosylation detection sites for wheat germ agglutinin are bis-GlcNAc and SA.

TRITC-lysine-dextran, 10kDa, is a dextran compound conjugated with lysine and contains the fluorescent group TRITC. Lysine-dextran exhibits a higher binding affinity to glutamic acid-plasminogen compared to dextran alone.

Cyanine3 carboxylic acid is a non-toxic red fluorescent dye that serves as a non-reactive fluorophore for experimental controls and calibration. It can also be conjugated with targeting active molecules to create fluorescent probes for rapid detection of molecular reactions. [Ex Em(nm)=550 570nm]

FITC-PEG-FA (MW 10000) is a fluorescent dye composed of Folic acid (FA), polyethylene glycol (PEG), and FITC. Through specific chemical reactions, fluorescein is conjugated with PEG and Folic acid, resulting in a molecule with unique properties. FITC-PEG-FA (MW 10000) is suitable for fluorescence labeling and imaging.

Chitosan-Cy7.5 (MW 100000) is chitosan conjugated with the Cy7.5 dye. This compound is applicable in fluorescence labeling and imaging.

MitoPerOx is a ratiometric fluorescent probe that can be used to assess changes in lipid peroxidation within mitochondria. It is composed of a BODIPY fluorophore conjugated via a dienyl link to a triphenylphosphonium cation component that drives its accumulation in mitochondria. MitoPerOx displays an excitation maximum of 495 nm and exhibits a shift in emission maxima from 590 to 520 nm upon mitochondrial lipid peroxidation, enabling determination of ratiometric measurements of lipid peroxidation in live cells.