You Searched For: Iodoacetamide

Supplier: Apollo Scientific

Description: Iodoacetamide 98%

Supplier: Merck

Description: Iodoacetamide for synthesis, Sigma-Aldrich®

MSDS

Catalog Number: (M216-30G)

Supplier: VWR Chemicals

Description: Iodoacetamide ≥98%, Proteomics Grade

UOM: 1 * 30 g

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Supplier: Thermo Scientific

Description: Iodoacetamide 98%

MSDS

Supplier: Thermo Scientific

Description: Alkylating agent used in peptide mapping because it covalently binds with the thiols in cysteine to prevent disulfide bond formation.

MSDS Certificates

Catalog Number: (407710-25)

Supplier: Merck Millipore (Calbiochem‎)

Description: Iodoacetamide, Millipore®

UOM: 1 * 25 g

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Supplier: Biotium

Description: MTS, TS and maleimide, and other thiol-modifying reagents and reactive fluorescent dyes.

Catalog Number: (RC-150)

Supplier: G-Biosciences

Description: Iodoacetamide

UOM: 1 * 25 g

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Catalog Number: (786-078)

Supplier: G-Biosciences

Description: Iodoacetamide

UOM: 1 * 24 items

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Catalog Number: (786-228)

Supplier: G-Biosciences

Description: Iodoacetamide

UOM: 1 * 5 g

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Catalog Number: (MOLE24815520-25G)

Supplier: Molekula

Description: Iodoacetamide

UOM: 1 * 25 g

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Supplier: MP Biomedicals

Description: Iodoacetamide is a thiol reagent; alkylating reagent for cysteine and histidine residues in proteins. In the alkylation reaction, it reacts with histidine (such as in RNase), methionine and sulfhydryl groups of many proteins.

Supplier: Biotium

Description: Biotium offers reactive biotin compounds with a variety of reactive functional groups.

Catalog Number: (PRSI92-481)

Supplier: ProSci Inc.

Description: Mouse Legumain,also known as LGMN, is a cysteine protease belonging to peptidase family C13 and is expressed in kidney and placenta abundantly. LGMN has a strict specificity for hydrolysis of asparaginyl bonds. It can also cleave aspartyl bonds slowly, especially under acidic conditions. The mammalian legumain is involved in the processing of proteins for MHC class II antigen presentation in the lysosomal/endosomal system. It plays a role in the regulation of cell proliferation via its role in EGFR degradation. Legumain deficiency causes the accumulation of pro-Cathepsins B, H and L, another group of lysosomal cysteine proteases. Overexpression of Legumain in tumours is significant for invasion/metastasis. Mammalian legumain is inhibited by iodoacetamide and maleimides. Legumain activation appears to be autocatalytic and can be triggered by acidic pH.

UOM: 1 * 50 µG

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Catalog Number: (786-232)

Supplier: G-Biosciences

Description: The FOCUS™ Protein Alkylation Kit is a proteomic grade iodoacetamide reagent kit for blocking thiols by alkylation. The kit is supplied with a proprietary buffer necessary for efficient alkylation of thiols, while minimising reoxidation of the competing thiol pairs in protein samples. Simply add an appropriate amount to reagent solutions for alkylation of protein thiol groups.

UOM: 1 * 1 KIT

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Supplier: MP Biomedicals

Description: Inhibitors: p-Chloromercuribenzoate, iodoacetamide, heavy metal ions (Zn²⁺, Fe²⁺, Zn²⁺, Cd²⁺, Cu²⁺, Pb²⁺, Ag⁺, Hg²⁺), ionic Detergents (SDS, DAC, etc.). Contaminants: The preparation is practically free from other glycosidases (a-galactosidase, a-,b-glucosidase, a-,b-mannosidase, etc.) and proteinase. Principle: o-Nitrophenyl-b-D-galactopyranoside (ONPG) b-galactosidase > o-Nitrophenol (ONP) + D-Galactose. The appearance of o-nitrophenol is measured at 410 nm by spectrophotemetry. Thermal Stability: Below 50 °C (pH 7,3; 15 min) (Lit.), Optimum Temperature: 50 to 55 °C (Lit.).