Specs:

 SDS

Molecular Weight: 504.53; single compound

CAS: 1334177-79-5

Purity: > 98%

Spacers: dPEG® Spacer is 28 atoms and 31.9 Å

Shipping: Ambient

References: Greg T. Hermanson, Bioconjugate Techniques, 2nd Edition, Elsevier Inc., Burlington, MA 01803, April, 2008 (ISBN-13: 978-0-12-370501-3; ISBN-10: 0-12-370501-0); See pp. 276-335 for general description and use of heterobifunctional crosslinkers, and the specific sample protocol for SMCC or sulfo-SMCC on pp. 283-286.

Greg T. Hermanson, Bioconjugate Techniques, 3rd Edition, Elsevier, Waltham, MA 02451, 2013, ISBN 978-0-12-382239-0; See Chapter 18, Discrete PEG Reagents, pp. 787-821, for a full overview of the dPEG® products.





Additional Search Phrases: PEG, dPEG, discrete PEG, polyethylene glycol, PEGylation reagent, crosslinker, crosslinkers, crosslinking reagent, crosslinking reagents, heterobifunctional crosslinker, amine reactive, thiol reactive, sulfhydryl reactive, maleimide, maleimido, carboxyl, carboxylic acid, propanoic acid, propionic acid, PEG6, MAL-PEG6-acid, MAL-PEG6-COOH, Carboxy-PEG6-maleimide, MAL-PEG-acid


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MAL dPEG®₆-acid

$125.00 – $150.00

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PRODUCT IS SOLD STRICTLY FOR INTERNAL LABORATORY AND RESEARCH PURPOSES ONLY AND HAS NOT BEEN REVIEWED BY THE FDA. PRODUCT IS NOT FOR RESALE AND CANNOT BE INCORPORATED INTO COMMERCIAL GOODS FOR ANY USE OR USED IN THE DEVELOPMENT OF COMMERCIAL PRODUCTS OR IN THE PERFORMANCE OF COMMERCIAL SERVICES UNLESS UNDER A SEPARATE LICENSING, SUPPLY, OR DISTRIBUTOR AGREEMENT WITH QUANTA BIODESIGN, LTD. For information pertaining to the commercial use of our products, please click here to contact us.

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Product#: 10065 Categories: , , Tags: , , , , , , , , , , , , , , , ,

MAL-dPEG®₆-acid, product number 10065, is a crosslinker that joins sulfhydryl groups to free amines through a single molecular weight polyethylene glycol (PEG) chain of discrete length. The maleimidopropyl moiety reacts with sulfhydryl groups via a Michael addition reaction. The propionic acid terminus of the molecule reacts directly with free amines using EDC or another carbodiimide to form amide bonds. Alternatively, activation of the propionic acid group with N-hydroxysuccinimide (NHS), 2,3,5,6-tetrafluorophenol (TFP), or some other acylating agent permits amide bond formation under mild, controlled conditions.

Additional information

Weight .5 oz
Dimensions .75 × .75 × 2 in

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