Protein Modification Reagents
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Filtered Search Results
Medchemexpress LLC Amine-PEG3-desthiobiotin | 2237234-71-6 | None | 99.9% | 388.50 g·mol⁻¹ | C18H36N4O5 | 5 MG
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Amine-PEG3-desthiobiotin is a short PEG-based linker with a terminal primary amine and a desthiobiotin affinity tag. It is designed for use in PROTAC synthesis and bioconjugation workflows where a removable biotin-like label and a short, flexible spacer are required.
- Provides a terminal primary amine for amide coupling.
- Contains a desthiobiotin tag for reversible affinity capture.
- Short PEG3 spacer reduces steric hindrance between ligands.
- High reported purity suitable for synthetic applications.
- Supplied as a solid for straightforward handling and storage.
- Compatible with common bioconjugation chemistries.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000669104 FITC-PEG-DBCO MW 50 25MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000669107 RHODAMINE-PEG MW 20 50MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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NC3991562 NH2-PEG3-C6-CL HYDROCHLORIDE
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Hampton Research HR2-428-43/Additive Screen 43 (D07), 1.0 ml - 1.0 M Guanidine hydrochloride
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HR2-428-43/Additive Screen 43 (D07), 1.0 ml - 1.0 M Guanidine hydrochloride. Please note items from this supplier are non-returnable.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000733410 BNO-PEG4-CH2COOH 500MG
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Medchemexpress LLC Alkyne-SNAP | 1104822-07-2 | C18H18N6O2 | 5 MG
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Alkyne-SNAP is an Alkyne-conjugated benzylguanine. The benzylguanine moiety reacts with the SNAP-tag, allowing irreversible and covalent labeling of SNAP fusion proteins with an additional alkyne functionality for further click chemistry conjugation.
- Alkyne-conjugated benzylguanine
- Reacts with SNAP-tag
- Enables irreversible and covalent labeling of SNAP fusion proteins
- Provides alkyne functionality for click chemistry conjugation
- Suitable for labeling and fluorescence imaging
- Useful in antibody-drug conjugate (ADC) related applications
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ABclonal Technology PLA2G7 Rabbit pAb
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The protein encoded by this gene is a secreted enzyme that catalyzes the degradation of platelet-activating factor to biologically inactive products. Defects in this gene are a cause of platelet-activating factor acetylhydrolase deficiency. Two transcript variants encoding the same protein have been found for this gene.
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ABclonal Technology HAS3 Rabbit pAb
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The protein encoded by this gene is involved in the synthesis of the unbranched glycosaminoglycan hyaluronan, or hyaluronic acid, which is a major constituent of the extracellular matrix. This gene is a member of the NODC/HAS gene family. Compared to the proteins encoded by other members of this gene family, this protein appears to be more of a regulator of hyaluronan synthesis. Alternative splicing results in multiple transcript variants.
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VECTOR LABORATORIES LLC SULFO DBCO-PEG4-TFP ESTER 500
502386106 SULFO DBCO-PEG4-TFP ESTER 500
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VECTOR LABORATORIES LLC BIOTIN-PEG4-DBCO 25 MG
502386968 BIOTIN-PEG4-DBCO 25 MG
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Medchemexpress LLC N-(Amino-PEG2)-N-bis(PEG3-azide) | 2606952-86-5 | 99.9% | 550.65 | 100 MG
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N-(Amino-PEG2)-N-bis(PEG3-azide) is a PEG-based PROTAC linker utilized in the synthesis of PROTACs. It functions as a click chemistry reagent due to its azide group, enabling copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with alkyne-containing molecules. It can also participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- Click chemistry reagent
- Contains an azide group
- Undergoes copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc)
- Reacts with molecules containing alkyne groups
- Undergoes strain-promoted alkyne-azide cycloaddition (SPAAC) reactions
- Reacts with molecules containing DBCO or BCN groups
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Medchemexpress LLC Amino-PEG4-CH2COOH | 195071-49-9 | ≥98.0% | 251.28 g/mol | C10H21NO6 | 250 MG
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Amino-PEG4-CH2COOH is a four-unit polyethylene glycol (PEG4) linker bearing a terminal amino group and a carboxylic acid (-CH2COOH). It is used as a hydrophilic spacer in bioconjugation chemistries such as PROTAC and antibody-drug conjugate (ADC) synthesis.
- Four-unit PEG spacer providing flexibility and solubility.
- Terminal amino and carboxylic acid functionalities for straightforward conjugation.
- High chemical purity suitable for research applications.
- Molecular weight approximately 251.28 g/mol, formula C10H21NO6.
- Available in common lab pack sizes, including 250 MG for small-scale synthesis.
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Medchemexpress LLC Dbco-peg4-pfp ester | 2182601-19-8 | 95.0% | C36H35F5N2O8 | 100 MG
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DBCO-PEG4-PFP ester is a PEG-based PROTAC linker utilized in the synthesis of PROTACs. It functions as a click chemistry reagent, containing a DBCO group that facilitates strain-promoted alkyne-azide cycloaddition (SPAAC) with azide-containing molecules. This allows it to leverage the intracellular ubiquitin-proteasome system for selective degradation of target proteins.
- Peg-based protac linker
- Utilized in protac synthesis
- Functions as a click chemistry reagent
- Contains a dbco group for spaac reactions
- Facilitates selective degradation of target proteins
- Appears as a colorless to light yellow oil
- Purity of 95.0%
- Molecular weight: 718.66
- Molecular formula: C36H35F5N2O8
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Medchemexpress LLC Fmoc-NH-PEG3-CH2CH2COOH | 867062-95-1 | MFCD06656471 | 99.8% | 443.49 g/mol | C24H29NO7 | 100 MG
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Fmoc-NH-PEG3-CH2CH2COOH is a PEG-based, Fmoc-protected heterobifunctional linker designed for use in antibody-drug conjugate (ADC) and proteolysis-targeting chimera (PROTAC) construction. It features an Fmoc-protected amine and a terminal carboxylic acid that enable standard peptide-coupling and conjugation chemistries.
- Fmoc-protected amine enabling orthogonal deprotection
- Terminal carboxylic acid for amide coupling
- Molecular formula C24H29NO7 and molecular weight 443.49 g/mol
- Cas number 867062-95-1
- Purity 99.8%
- Available in small-scale packages such as 100 MG
- Storage: pure form -20°C (3 years) or 4°C (2 years); in solvent -80°C (6 months)
- Suitable for ADC and PROTAC linker synthesis and bioconjugation
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