Catalog |
name |
Description |
price |
R-M-7070 |
BBTDT-BT-TPA |
BBTDT-BT-TPA is a near-infrared dye, which can be used for near-infrared two zone fluorescence imaging. |
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R-M-7071 |
TTQ-BT-TPA |
TTQ-BT-TPA is a near-infrared dye, which can be used for near-infrared two zone fluorescence imaging. |
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R-M-7072 |
TTQF-Q |
TTQF-Q is a near-infrared dye, which can be used for near-infrared two zone fluorescence imaging. |
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R-M-7073 |
TTQF-SO3 |
TTQF-SO3 is a near-infrared dye, which can be used for near-infrared two zone fluorescence imaging. |
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R-M-7074 |
TTQ-2TC |
TTQ-2TC is a near-infrared dye, which can be used for near-infrared two zone fluorescence imaging. |
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R-M-7075 |
BT-BBT-2TC |
BT-BBT-2TC is a near-infrared dye, which can be used for near-infrared two zone fluorescence imaging. |
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R-M-7076 |
TTQ-2TC-4T |
TTQ-2TC-4T is a near-infrared dye, which can be used for near-infrared two zone fluorescence imaging. |
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R-M2xa-9815 |
IR820-COOH |
IR820-COOH is a near-infrared (NIR) fluorescent dye derivative in which IR820 (a heptamethine cyanine dye similar to indocyanine green, ICG) is chemically modified to introduce a carboxyl (-COOH) group for conjugation or functionalization.
Applications:
Photothermal therapy (PTT): Converts NIR light to heat for tumor ablation.
Fluorescence imaging: For in vivo tumor visualization and biodistribution studies.
Photoacoustic imaging: Dual-mode imaging when integrated into nanocarriers.
Drug delivery systems: As a functional probe to track or activate nanocarriers. |
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R-M2cq-9816 |
IR820-HA MW:40k |
IR820-HA MW:40k/IR820-HA40k/IR820-hyaluronic acid40000 is a hyaluronic acid (HA)-conjugated near-infrared (NIR) probe.
Applications:
Targeted photothermal therapy (PTT) for tumors or inflammatory tissues.
NIR fluorescence and photoacoustic imaging of CD44-positive lesions.
Theranostic nanocarrier component when further incorporated into nanoparticles or liposomes. |
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R-M2xa-9817 |
IR820-NH2 |
IR820-NH2 is a near-infrared (NIR) fluorescent dye derived from the heptamethine cyanine dye IR820, functionalized with a primary amine (-NH₂) group. This modification enables further chemical coupling via amide, urea, or thiourea bond formation, making it a versatile building block for bioconjugation.
Applications
Conjugation to carboxyl-containing biomolecules (e.g., hyaluronic acid, peptides, proteins).
Liposome and nanoparticle surface modification for NIR fluorescence and photothermal functions.
Dual-function theranostic agents when combined with targeting ligands or therapeutic molecules.
Fluorescent probes for imaging and biodistribution studies. |
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