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Results for "

tamra-peg-3-azide

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TAMRA-PEG3-Azide
T169821228100-59-1
TAMRA-PEG3-Azide is a TAMRA red fluorescent dye linker with a maximum excitation emission wavelength of 553 575 nm.
  • $143
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(5,6)TAMRA-PEG3-Azide-PEG3-Desthiobiotin
T17339
(5,6)TAMRA-PEG3-Azide-PEG3-Desthiobiotin is a polyethylene glycol (PEG)-based PROTAC linker used for the synthesis of PROTACs.
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DOTA-(t-butyl)3-PEG5-azide
T17846
DOTA-(t-butyl)3-PEG5-azide is a polyethylene glycol (PEG)-derived linker specifically designed for the synthesis of proteolysis targeting chimeras (PROTACs)[1].
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m-PEG-azide (MW 10000)
T18082
m-PEG-azide (MW 10000), a PEG-based linker for PROTACs, joins two essential ligands crucial for forming PROTAC molecules, enabling selective protein degradation through the ubiquitin-proteasome system within cells.
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m-PEG-azide (MW 2000)
T18083
m-PEG-azide (MW 2000) is a PEG-based linker used in PROTACs to join two essential ligands, facilitating the selective degradation of target proteins through the ubiquitin-proteasome system within cells.
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DBCO-(PEG)3-VC-PAB-MMAE
T17817
DBCO-(PEG)3-VC-PAB-MMAE is a chemical compound where monomethyl auristatin E (MMAE), a potent tubulin inhibitor used as a toxin payload in antibody-drug conjugates, is conjugated via a DBCO-(PEG)3-vc-PAB linker.
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m-PEG-azide (MW 5000)
T18085
m-PEG-azide (MW 5000) is a PEG-based linker for PROTACs, facilitating the conjugation of two essential ligands to enable selective protein degradation via the ubiquitin-proteasome system in cells.
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Azide-PEG-azide (MW 2000)
T17461
Azide-PEG-azide (MW 2000) is a polyethylene glycol (PEG)-based linker used for synthesizing proteolysis-targeting chimeras (PROTACs)[1].
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Azide-PEG-alcohol (MW 2000)
T17456
Azide-PEG-alcohol, a polyethylene glycol (PEG)-based PROTAC linker with a molecular weight of 2000, functions as a versatile option for the synthesis of PROTACs[1].
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Azide-PEG-amine (MW 2000)
T17457
Azide-PEG-amine (MW 2000) is a Polyethylene Glycol (PEG)-derived linker compound used in the synthesis of Proteolysis Targeting Chimeras (PROTACs)[1].
  • $68
5 days
Size
QTY
m-PEG-azide (MW 20000)
T18084
m-PEG-azide (MW 20000) is a PEG-based linker for PROTACs, facilitating the connection of two essential ligands necessary for forming PROTAC molecules, thereby enabling selective protein degradation through the ubiquitin-proteasome system within cells.
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Azide-PEG-amine (MW 5000)
T17459
Azide-PEG-amine (MW 5000) is a polyethylene glycol (PEG)-derived linker compound with azide functionality, primarily utilized in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].
    Inquiry
    Azide-PEG-azide (MW 10000)
    T17460
    Azide-PEG-azide (MW 10000) is a polyethylene glycol (PEG)-based linker essential for PROTACs synthesis and assembly[1].
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    Azide-PEG-azide (MW 5000)
    T17463
    Azide-PEG-azide (MW 5000) is a polyethylene glycol (PEG)-based linker component employed in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].
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    Pyrene azide 3
    T397822252168-06-0
    Pyrene azide 3 is a PEG-based linker for PROTACs, facilitating the connection between two essential ligands to form PROTAC molecules, thereby enabling selective protein degradation via the ubiquitin-proteasome system within cells.
    • $1,520
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    TAMRA-Azide-PEG-biotin
    T169811797415-74-7
    TAMRA-Azide-PEG-biotin is a PEG-based linker for PROTACs, joining two essential ligands. This linker facilitates selective protein degradation by utilizing the ubiquitin-proteasome system within cells.
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    Azide-PEG-azide (MW 20000)
    T17462
    Azide-PEG-azide (MW 20000) is a polyethylene glycol (PEG)-based linker compound used in the synthesis of Proteolysis Targeting Chimeras (PROTACs)[1].
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    Azide-PEG-amine (MW 3500)
    T17458
    Azide-PEG-amine (MW 3500) is a polyethylene glycol (PEG) linker compound, designed for the synthesis of proteolysis targeting chimeric molecules (PROTACs)[1].
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    Biotin-PEG4-Dde-TAMRA-PEG3-Azide
    T175842353409-56-8
    Biotin-PEG4-Dde-TAMRA-PEG3-Azide is a seven-unit polyethylene glycol (PEG) linker used in the synthetic production of antibody-drug conjugates (ADCs) and is cleavable[1].
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