8 Results for "

transmembrane pore

" in MedChemExpress (MCE) Product Catalog:
Products (8)

8 Results for "transmembrane pore" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-135416
CAS No.: 98072-47-0
Streptolysin O is a cholesterol-targeting, thiol-activated pore-forming toxin. Streptolysin O binds to cholesterol via its C-terminal domain 4, oligomerizes to form arc-shaped or ring-shaped structures, inserts amphipathic helices into the lipid bilayer, and forms transmembrane β-barrel pores, resulting in cell permeabilization. Streptolysin O enables controllable cell membrane permeabilization, fluorescent probe delivery, and exogenous molecule uptake .
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1
1 Cited Publications
Cat. No.: HY-135416A
CAS No.: 98072-47-0
Purity:  ≥96.0%
Recombinant Streptolysin O is a cholesterol-targeting, thiol-activated pore-forming toxin. Recombinant Streptolysin O binds to cholesterol via its C-terminal domain 4, oligomerizes to form arc-shaped or ring-shaped structures, inserts amphipathic helices into the lipid bilayer, and forms transmembrane β-barrel pores, resulting in cell permeabilization. Recombinant Streptolysin O enables controllable cell membrane permeabilization, fluorescent probe delivery, and exogenous molecule uptake .
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Cat. No.: HY-P4119
CAS No.: 863608-35-9
Research Areas:  

Others

Pep-1-Cysteamine is an amphipathic chimeric cell-penetrating peptide. Pep-1-Cysteamine can penetrate biological membranes in an energy-independent manner without forming transmembrane pores, and efficiently deliver active proteins into cells, with its translocation dominated by electrostatic interactions and membrane perturbation .
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Cat. No.: HY-157343
CAS No.: 62010-37-1
GD3 Ganglioside is an Apoptosis inducer and a biomarker for mouse neural stem cells. GD3 Ganglioside expresses in neural stem cells and the subventricular zone of the adult mouse brain. GD3 Ganglioside targets the mitochondrial permeability transition pore complex, induces pore opening, dissipates mitochondrial transmembrane potential, triggers Mitochondrial swelling, releases pro-apoptotic factors, and activates Caspase-9. GD3 Ganglioside is applicable to research related to glioblastoma .
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Cat. No.: HY-157343A
GD3 Ganglioside sodium is an Apoptosis inducer and biomarker for mouse neural stem cells. GD3 Ganglioside sodium expresses in neural stem cells and the subventricular zone of the adult mouse brain. GD3 Ganglioside sodium targets the mitochondrial permeability transition pore complex, induces pore opening, dissipates mitochondrial transmembrane potential, triggers Mitochondrial swelling, releases pro-apoptotic factors, and activates Caspase-9. GD3 Ganglioside sodium is applicable to research related to glioblastoma .
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Cat. No.: HY-157343B
GD3 Ganglioside ammonium is an Apoptosis inducer and biomarker for mouse neural stem cells. GD3 Ganglioside ammonium expresses in neural stem cells and the subventricular zone of the adult mouse brain. GD3 Ganglioside ammonium targets the mitochondrial permeability transition pore complex, induces pore opening, dissipates mitochondrial transmembrane potential, triggers Mitochondrial swelling, releases pro-apoptotic factors, and activates Caspase-9. GD3 Ganglioside ammonium is applicable to research related to glioblastoma .
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Cat. No.: HY-P4105
Research Areas:  

Others

TAT (47-57), TAMRA-labeled is a fluorescently labeled cell-penetrating peptide derived from the HIV-1 transactivator of transcription (TAT). TAT (47-57), TAMRA-labeled is conjugated to the red fluorescent dye carboxytetramethylrhodamine (TAMRA, with an absorption/emission wavelength of approximately 541/568 nM). TAT (47-57), TAMRA-labeled can be used in studies related to cellular uptake, translocation and drug delivery .
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Cat. No.: HY-P4105A
Research Areas:  

Others

TAT (47-57), TAMRA-labeled acetate is a fluorescently labeled cell-penetrating peptide derived from the HIV-1 transactivator of transcription (TAT). TAT (47-57), TAMRA-labeled acetate is conjugated to the red fluorescent dye carboxytetramethylrhodamine (TAMRA, with an absorption/emission wavelength of approximately 541/568 nM). TAT (47-57), TAMRA-labeled acetate can be used in studies related to cellular uptake, translocation and drug delivery .
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