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15356 results for "Acryloyl+PEG+amine&amp"

15356 Results for: "Acryloyl+PEG+amine&amp"

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(2E)-3-(2-Chlorophenyl)acryloyl chloride

(2E)-3-(2-Chlorophenyl)acryloyl chloride

Supplier: Matrix Scientific

Matrix Scientific Part Number: 062324-500MG , MDL Number: MFCD00039311

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(2E)-3-(4-Isopropylphenyl)acryloyl chloride

(2E)-3-(4-Isopropylphenyl)acryloyl chloride

Supplier: Matrix Scientific

Matrix Scientific Part Number: 062331-500MG , MDL Number: MFCD11107996

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8-Arm PEG Biotin

Supplier: ALADDIN SCIENTIFIC

4 arm PEG derivatives have multiple reactive groups that can be used to modify proteins, peptides and other materials via their functional groups. PEGylation can increase solubility and stability and reduce immunogenicity of peptides and proteins. It can also suppress the non-specific binding of charged molecules to the modified surfaces. .

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(2E)-3-(2-Furyl)acryloyl chloride

(2E)-3-(2-Furyl)acryloyl chloride

Supplier: Matrix Scientific

Matrix Scientific Part Number: 062322-500MG , MDL Number: MFCD00673695

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(2E)-3-(4-Nitrophenyl)acryloyl chloride

(2E)-3-(4-Nitrophenyl)acryloyl chloride

Supplier: Matrix Scientific

Matrix Scientific Part Number: 062333-500MG , MDL Number: MFCD00082549

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4-Arm PEG DTPA

Supplier: ALADDIN SCIENTIFIC

4 arm PEG derivatives have multiple reactive groups that can be used to modify proteins, peptides and other materials via their functional groups. PEGylation can increase solubility and stability and reduce immunogenicity of peptides and proteins. It can also suppress the non-specific binding of charged molecules to the modified surfaces. .

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8-Arm PEG NHS

Supplier: ALADDIN SCIENTIFIC

8 arm PEG derivatives have multiple reactive groups that can be used to modify proteins, peptides and other materials via their functional groups. PEGylation can increase solubility and stability and reduce immunogenicity of peptides and proteins. It can also suppress the non-specific binding of charged molecules to the modified surfaces. .

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8-Arm PEG Biotin

Supplier: ALADDIN SCIENTIFIC

4 arm PEG derivatives have multiple reactive groups that can be used to modify proteins, peptides and other materials via their functional groups. PEGylation can increase solubility and stability and reduce immunogenicity of peptides and proteins. It can also suppress the non-specific binding of charged molecules to the modified surfaces. .

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Azido PEG NHS ≥95%

Supplier: ALADDIN SCIENTIFIC

Amino functionalized methoxyl polyethylene glycol, amino PEG (mPEG-NH2) is a mono reactive PEG derivative that can be used to modify proteins, peptides and other materials via carboxylic group (-COOH) or other amine reactive chemical groups. PEGylation can increase solubility and stability and reduce immunogenicity of peptides and proteins. It can also suppress the non-specific binding of charged molecules to the modified surfaces.

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(2E)-3-(4-Methoxyphenyl)acryloyl chloride

(2E)-3-(4-Methoxyphenyl)acryloyl chloride

Supplier: Matrix Scientific

Matrix Scientific Part Number: 062330-500MG , MDL Number: MFCD00039314

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Acrylate PEG Biotin

Supplier: ALADDIN SCIENTIFIC

8 arm PEG derivatives have multiple reactive groups that can be used to modify proteins, peptides and other materials via their functional groups. PEGylation can increase solubility and stability and reduce immunogenicity of peptides and proteins. It can also suppress the non-specific binding of charged molecules to the modified surfaces. .

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8-Arm PEG Thiol

Supplier: ALADDIN SCIENTIFIC

8 arm PEG derivatives have multiple reactive groups that can be used to modify proteins, peptides and other materials via their functional groups. PEGylation can increase solubility and stability and reduce immunogenicity of peptides and proteins. It can also suppress the non-specific binding of charged molecules to the modified surfaces. .

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2-[3-(4-Nitrophenyl)acryloyl]benzenecarboxylic acid ≥95%

2-[3-(4-Nitrophenyl)acryloyl]benzenecarboxylic acid ≥95%

Supplier: Matrix Scientific

Matrix Scientific Part Number: 045964-5G , MDL Number: MFCD03617865

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Acrylate PEG Biotin ≥95%

Supplier: ALADDIN SCIENTIFIC

8 arm PEG derivatives have multiple reactive groups that can be used to modify proteins, peptides and other materials via their functional groups. PEGylation can increase solubility and stability and reduce immunogenicity of peptides and proteins. It can also suppress the non-specific binding of charged molecules to the modified surfaces. .

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(2E)-3-(2,4-Dichlorophenyl)acryloyl chloride

(2E)-3-(2,4-Dichlorophenyl)acryloyl chloride

Supplier: Matrix Scientific

Matrix Scientific Part Number: 062336-500MG , MDL Number: MFCD09752199

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4-Arm PEG Aspartic Acid

Supplier: ALADDIN SCIENTIFIC

Nanocs' amino acid and peptide PEG conjugates were made from the covalent attachment of PEG to various amino acid derivatives. Conjugates were provided in lyophilized powder form.

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(2E)-3-(5-Methyl-2-furyl)acryloyl chloride 95%

Supplier: Ambeed

(2E)-3-(5-Methyl-2-furyl)acryloyl chloride, Purity: 95%, CAS number: 111252-41-6, Appearance: Solid or liquid, Storage: Inert atmosphere, 2-8C, Size: 1G

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Adenosine 5'-monophosphate disodium salt (AMP disodium salt) ≥98% (by HPLC)

Supplier: Enzo Life Sciences

Adenosine 5'-monophosphate disodium salt (AMP disodium salt) ≥98% (by HPLC)

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AMP (2-Amino-2-methylpropanol), (max. 5% H₂O) 95%

Supplier: Thermo Scientific Chemicals

100ML

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Alkyne PEG acid

Supplier: ALADDIN SCIENTIFIC

Alkyne PEG acid

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4-Arm PEG Aspartic Acid

Supplier: ALADDIN SCIENTIFIC

Nanocs' amino acid and peptide PEG conjugates were made from the covalent attachment of PEG to various amino acid derivatives. Conjugates were provided in lyophilized powder form.

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2-Arm/Branched PEG Biotin

Supplier: ALADDIN SCIENTIFIC

2 arm PEG derivatives have two PEG branches with one or two functional groups that can be used to modify proteins, peptides and other materials via their functional groups. PEGylation can increase solubility and stability and reduce immunogenicity of peptides and proteins. It can also suppress the non-specific binding of charged molecules to the modified surfaces. .

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Alkyne PEG acid

Supplier: ALADDIN SCIENTIFIC

Alkyne PEG acid

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4-Arm PEG vinyl sulphone

Supplier: ALADDIN SCIENTIFIC

4 arm PEG derivatives have multiple reactive groups that can be used to modify proteins, peptides and other materials via their functional groups. PEGylation can increase solubility and stability and reduce immunogenicity of peptides and proteins. It can also suppress the non-specific binding of charged molecules to the modified surfaces. .

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(2E)-3-(4-tert-Butylphenyl)acryloyl chloride

(2E)-3-(4-tert-Butylphenyl)acryloyl chloride

Supplier: Matrix Scientific

Matrix Scientific Part Number: 062332-500MG , MDL Number: MFCD11108006

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N-Biotinyl-NH-(PEG)2-COOH DIPEA ≥95% (by HPLC)

Supplier: Adipogen

Functionalized biotin. Biotinylated polyethylene glycol (PEG-Biotin) is an avidine or streptavidin reactive PEG derivative that can be used to modify biomolecues or other surfaces through biotin-streptavidin interaction. Used for addition of biotin-PEG to the N-terminus of resin-bound peptides. Can be introduced using standard coupling methods, such as PyBOP or TBTU and has better solubility in DMF and NMP than comparable non-PEG-containing derivatives, such as biotin-Ahx and biocytin.

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4-Arm PEG vinyl sulphone

Supplier: ALADDIN SCIENTIFIC

4 arm PEG derivatives have multiple reactive groups that can be used to modify proteins, peptides and other materials via their functional groups. PEGylation can increase solubility and stability and reduce immunogenicity of peptides and proteins. It can also suppress the non-specific binding of charged molecules to the modified surfaces. .

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Azido PEG Biotin ≥95%

Supplier: ALADDIN SCIENTIFIC

Azide/azido functionalized polyethylene glycol (N3-PEG-X) is a bifunctional PEG derivative that can be used to modify proteins, peptides and other materials. Azide group can react with alkyne in aqueous solution catalyzed by copper. It can also be reduced into amine group easily while another functional group can be react with other molecules or functional groups. PEGylation can increase solubility and stability and reduce immunogenicity of peptides and proteins. It can also suppress the non-specific binding of charged molecules to the modified surfaces.

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