Protein Modification Reagents
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Filtered Search Results
Sigma Aldrich Fine Chemicals Biosciences Collagenase P from Clostridium histolyticum |
Collagenase P from Clostridium histolyticum |
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Medchemexpress LLC 4,7,10,13-tetraoxapentadecanoic acid, 15-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)- | 518044-36-5 | 99.9% | 1 G
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Mal-PEG4-Boc is a PEG-based PROTAC linker suitable for research applications. It has a molecular formula of C19H31NO8 and a molecular weight of 401.45. It appears as a colorless to light yellow oil. This product is for research use only and has not been fully validated for medical applications.
- Peg-based protac linker
- For research use only
- Molecular formula: C19H31NO8
- Molecular weight: 401.45
- Colorless to light yellow oil appearance
- Store at -20°C under nitrogen
- In solvent, store at -80°C for 6 months or -20°C for 1 month under nitrogen
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STEMCELL Technologies Collagenase Type I, Size: 100 mg
Collagenase is a protease consisting of a single polypeptide chain approximately 1,000 amino acid residues in length. Collagenase is capable of digesting native collagen fibrils commonly found in connective tissues and therefore is frequently used for tissue dissociation. Collagenase Type I contains the activity of several proteases, including collagenase, caseinase, clostripain, and trypsin. Collagenase Type I has been used for the digestion of human tissues such as intestine (Barthel et al.), mammary glands (Huss & Kratz), and prostate (Le et al.), as well as specific cell types such as endothelial cells (Ganguly et al.) and dorsal root ganglion cells (Dib-Hajj et al.).
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Purepeg LLC MPEG36-N3 250L
MPEG36-N3 250L
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Chemscene ChemScene | Azido-PEG2-C2-acid | 5G | CS-0114500 | 0.97 | 1312309-63-9| MFCD20926378 | 203.2
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ChemScene | Azido-PEG2-C2-acid | 5G | CS-0114500 | 0.97 | 1312309-63-9| MFCD20926378 | 203.2
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Medchemexpress LLC 17-azido-3,6,9,12,15-pentaoxaheptadecyl 4-methylbenzenesulfonate | 906007-10-1 | MFCD29918254 | 98.6% | C19H31N3O8S | 10MG
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Azide-PEG6-Tos is an azide-functionalized PEG6 tosylate linker for bioconjugation and PROTAC synthesis. It supplies an azide reactive handle and a tosyl leaving group for downstream functionalization, facilitating click chemistry and linker assembly in small-molecule and bioconjugate research.
- High purity of 98.6% suitable for synthetic applications.
- Azide functional group enables copper-catalyzed and strain-promoted click reactions.
- Tosylate leaving group allows facile nucleophilic substitution and modification.
- PEG6 spacer provides flexibility and improves solubility in polar solvents.
- Liquid form, colorless to light yellow, for easy handling and dosing.
- Stable when stored under recommended conditions to maintain integrity.
- Available in small milligram sizes for discovery and linker development.
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MOLECULAR DIMENSIONS INC W/V PEG 6000
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NC3590321 W/V PEG 6000
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Grainger SINGL-E CLSS 47/64 MAX 100PK
NC3666428 SINGL-E CLSS 47/64 MAX 100PK
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Purepeg LLC MPEG11-OH 1GL
MPEG11-OH 1GL
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Purepeg LLC MALEIMIDE-NH-PEG2-CH2CH2COONHS 1L
MALEIMIDE-NH-PEG2-CH2CH2COONHS 1L
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Purepeg LLC 233436 HO-PEG36-OH 250mg
HO-PEG36-OH, M.F.: C72H146O37, M.W.: 1603.91, CAS # N/A
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Purepeg LLC MPEG8-NH2 250L
MPEG8-NH2 250L
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Purepeg LLC 432208 H2N-PEG8-CH2CH2COOH 250H
432208 H2N-PEG8-CH2CH2COOH 250H
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Purepeg LLC BOC-NH-PEG6-CH2CH2COOH 250MGL
BOC-NH-PEG6-CH2CH2COOH 250MGL
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Medchemexpress LLC Propargyl-PEG6-N3 | 1198080-03-3 | 100 MG
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Propargyl-PEG6-N3 is a PEG-based PROTAC linker employed in the synthesis of PROTACs. It functions as a versatile click chemistry reagent, featuring an Azide group. This group readily participates in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) when combined with molecules containing Alkyne groups. Furthermore, it can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules that possess DBCO or BCN groups, offering flexible synthetic pathways.
- PEG-based PROTAC linker.
- Used in the synthesis of PROTACs.
- Click chemistry reagent.
- Contains an Azide group.
- Participates in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with Alkyne groups.
- Undergoes strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups.
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