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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
114 Results for "
SnO2 plate electrodes
" in MedChemExpress (MCE) Product Catalog:
Products (114)
114 Results for "SnO2 plate electrodes" in MCE Product Catalog:
19
19 Publications Verification
Art. -Nr.: HY-P7114
Reinheit: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: RSPO1; R-Spondin Homolog (Xenopus Laevis); R-Spondin 1; R-Spondin Homolog; Roof plate-Specific Spondin-1; CRISTIN3; R-Spondin-1; HRspo1; FLJ40906; RSPO; RSPONDIN
Species:
Human
Source:
CHO
11
3
3 Cited Publications
Art. -Nr.: HY-P76012
Reinheit: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: RSPO1; R-Spondin Homolog (Xenopus Laevis); R-Spondin 1; R-Spondin Homolog; Roof plate-Specific Spondin-1; CRISTIN3; R-Spondin-1; HRspo1; FLJ40906; RSPO; RSPONDIN
Species:
Mouse
Source:
CHO
2
2 Cited Publications
2
2 Cited Publications
Synonyms: γ-Aminopropyltriethoxysilane; APTES
1
Collagenase, Type VI (EC 3.4.24.3) is a collagenase that can degrade type VI collagen. Type VI collagen is a component of cell membranes in various tissues (such as skin, heart, blood vessels, cartilage, and synovial fluid). Excessive collagenase can cause extracellular matrix lesions. Collagenase is also a biomarker for tumor invasion and metastasis. Collagenase, Type VI can specifically act on the peptide bond between proline and glycine. This feature can be used to quickly and sensitively detect its concentration level in experiments using corresponding modified electrodes .
1
Category:
Flavonols Plant Flavonoids Monophenols Phenols Other Families Extract Disease Research Fields Inflammation/Immunology
Target:
1
1 Cited Publications
Art. -Nr.: HY-W077680
CAS. Nr.: 1126-58-5
Target:
Forschungsgebiete:
Girard's P reagent is a reagent used in organic chemistry. Girard's P reagent is used to react with vanillin to form a hydrazone derivative, which is then combined with an ion selective electrode (ISE) to develop a potentiometric method for the determination of vanillin. Girard's P reagent can be used in the development of ion selective electrodes and in the study of organic analysis .
1
1 Cited Publications
Art. -Nr.: HY-P72784
Reinheit: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: RSPO1; R-Spondin Homolog (Xenopus Laevis); R-Spondin 1; R-Spondin Homolog; Roof plate-Specific Spondin-1; CRISTIN3; R-Spondin-1; HRspo1; FLJ40906; RSPO; RSPONDIN
Species:
Human
Source:
HEK293
1
1 Cited Publications
Art. -Nr.: HY-P700255
Reinheit: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: RSPO1; R-Spondin Homolog (Xenopus Laevis); R-Spondin 1; R-Spondin Homolog; Roof plate-Specific Spondin-1; CRISTIN3; R-Spondin-1; HRspo1; FLJ40906; RSPO; RSPONDIN
Species:
Mouse
Source:
E. coli
1
1 Cited Publications
Art. -Nr.: HY-P72784A
Reinheit: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: RSPO1; R-Spondin Homolog (Xenopus Laevis); R-Spondin 1; R-Spondin Homolog; Roof plate-Specific Spondin-1; CRISTIN3; R-Spondin-1; HRspo1; FLJ40906; RSPO; RSPONDIN
Species:
Human
Source:
HEK293
Art. -Nr.: HY-W015816
CAS. Nr.: 527-61-7
Synonyms: 2,6-DMBQ
Target:
Forschungsgebiete:
2,6-Dimethylbenzoquinone (2,6-DMBQ) is a benzoquinone derivative. 2,6-Dimethylbenzoquinone promotes Photosystem II-mediated photoelectrochemical water oxidation via electron transfer between spinach chloroplast Photosystem II membranes and carbon paste electrodes, and accepts electrons from Photosystem II during oxygen evolution assays. 2,6-Dimethylbenzoquinone undergoes direct photolysis in aqueous solution under 365 nm conditions, producing 2,6-dimethylhydroquinone and 3-hydroxy-2,6-dimethylbenzoquinone [2].
Forschungsgebiete:
Trifluralin is a selective, preemergence, soil-applied herbicide providing control of many important annual grass and broadleaf weed species. Trifluralin prevents weed growth by inhibiting root development through the interruption of mitosis. Trifluralin binds to tubulin and results in the failure of spindle apparatus and cell plate formation. Trifluralin inhibits radicle development on roots. Trifluralin inhibits cell mitosis. Trifluralin is considered to be neurotoxic and haematotoxic [2] .
Art. -Nr.: HY-Y1219H
CAS. Nr.: 112926-00-8
Art. -Nr.: HY-W008270
CAS. Nr.: 497-23-4
Synonyms: γ-Crotonolactone
Target:
Art. -Nr.: HY-W127790
CAS. Nr.: 52746-49-3
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
