Protein Modification Reagents
Biolegend LEAFTM Purified anti-human TIM
LEAF™ Purified anti-human TIMP-1 [Poly5296]; Isotype: Goat Polyclonal IgG; Reactivity: Human; Apps: Neut, IHC-P, WB; Size: 100 μg
eMolecules (S, R, S)-AHPC-PEG3-acid | | | 500mg
Broadpharm | (S, R, S)-AHPC-PEG3-acid | 500mg | 528284338 | BP-24504 | 98.000 | | | 662.800 | C32H46N4O9S
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eMolecules 17-(Bromoacetamido-PEG9-ethylcarbamoyl)heptadecanoic t-butyl ester | | | 250mg
Broadpharm | 17-(Bromoacetamido-PEG9-ethylcarbamoyl)heptadecanoic t-butyl ester | 250mg | 550804667 | BP-24488 | | | | 930.069 | C44H85BrN2O13
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eMolecules DBCO-C2-PEG4-amine | | | 100mg
Broadpharm | DBCO-C2-PEG4-amine | 100mg | 550804606 | BP-24374 | 98.000 | | | 595.693 | C32H41N3O8
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TARGETMOL CHEMICALS INC DBCO-PEG4-Biotin 10MG
Also available in 1 mg, 5 mg and bulk. Please contact Fisher for quotes. DBCO-PEG4-Biotin (ADIBO-NH-PEG2-Biotin) is an azadibenzocyclooctyne-biotin derivative containing a biotin moiety and 4 PEGs.DBCO-PEG4-Biotin is a versatile biotinylation reagent that introduces a portion of biotin into an azide-labelled biomolecule via a copper-free catalytic alkyl azide reaction (SPAAC). azide-labelled biomolecules via a copper-free catalytic alkyl azide reaction (SPAAC). Purity 96.19%
Medchemexpress LLC DOTA-PEG5-amine | 98.0% | 666.76 | 5 MG
DOTA-PEG5-amine is a PEG-based PROTAC linker, appearing as a white to off-white solid. It has a molecular weight of 666.76 and a chemical formula of C28H54N6O12. This linker can be utilized in the synthesis of PROTACs, which are small molecules designed to selectively degrade target proteins by exploiting the intracellular ubiquitin-proteasome system.
- Purity: 98.0%
- Form: Solid
- Color: White to off-white
- Intended for research use only
![Medchemexpress LLC Propanamide, N-[cis-4-[2-[[4-[4-[6-[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1-oxo-1H-isoindol-5-yl] | 2953426-43-0 | 98.0% | 855.98 | C47H53N9O7 | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000222303.png-250.jpg)
Medchemexpress LLC Propanamide, N-[cis-4-[2-[[4-[4-[6-[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1-oxo-1H-isoindol-5-yl] | 2953426-43-0 | 98.0% | 855.98 | C47H53N9O7 | 5 MG
A threonine tyrosine kinase (TTK)-targeting PROTAC degrader developed for research use, showing potent target degradation in cancer cell lines and antitumor activity in xenograft models. Supplied as a light yellow solid with documented analytical and storage data.
- Potent TTK degradation with reported DC50 values of 1.7 nM (COLO-205) and 5.8 nM (HCT-116).
- High reported purity of 98.01%.
- Molecular weight 855.98 and formula C47H53N9O7.
- Available in small-molecule quantities, including 5 mg solid format.
- Recommended storage: 4°C protected from light; in solvent: -80°C (6 months) or -20°C (1 month).
Medchemexpress LLC Mal-PEG2-VCP-Eribulin | 2130869-18-8 | 99.8% | 1374.57 | 5 MG
Mal-PEG2-VCP-Eribulin is a drug-linker conjugate for ADCs, combining an ADCs linker (Mal-PEG2-VCP) with Eribulin. Eribulin is a mechanistically unique microtubule inhibitor that inhibits the proliferation of cancer cells by binding to microtubule proteins and microtubules. This Eribulin-based agent is designed for antibody conjugates and is intended for research use only.
- Drug-linker conjugate for ADCs
- Contains ADCs linker (Mal-PEG2-VCP)
- Incorporates Eribulin, a microtubule inhibitor
- Inhibits cancer cell proliferation
- Suitable for antibody conjugates
- For research use only
ABclonal Technology KO Validated GSK3a Rabbit mAb
This gene encodes a multifunctional Ser Thr protein kinase that is implicated in the control of several regulatory proteins including glycogen synthase and transcription factors such as JUN It also plays a role in the WNT and PI3K signaling pathways as well as regulates the production of beta-amyloid peptides associated with Alzheimer s disease