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Dulaglutide Biosimilar – Anti-Glucagon-like peptide-1 receptor agonist mAb – Research Grade

Reference:
Product Image
SDS-PAGE for Dulaglutide Biosimilar - Anti-Glucagon-like peptide-1 receptor agonist mAb
Product Image
SDS-PAGE for Dulaglutide Biosimilar - Anti-Glucagon-like peptide-1 receptor agonist mAb
Size

100ug, 1MG
Isotype

hG4-Fc
Brand

ProteoGenix
Product type

Primary Antibodies
Clonality

Monoclonal Antibody
Expression system

Mammalian cells
Applications

Elisa, WB
Tags:
Specification
Description
Documents
QC & Validation Data1
Reviews
Product nameDulaglutide Biosimilar - Anti-Glucagon-like peptide-1 receptor agonist mAb - Research Grade
SourceDrugBank DB09045
SpeciesHuman
Expression systemMammalian cells
Molecular weight59kDa
Purity>85%
BufferPBS pH7.5
Delivery conditionBlue ice (+4°C)
Delivery Time3-5 days if in stock; 3-5 weeks if production needed
Storage condition4°C for short term; -20°C for long term
BrandProteoGenix
Aliases /SynonymsDulaglutide,Dulaglutide,Glucagon-like peptide-1 receptor agonist,anti-Glucagon-like peptide-1 receptor agonist
ReferencePX-TA1017
NoteFor research use only. Not suitable for clinical or therapeutic use.
IsotypehG4-Fc
ClonalityMonoclonal Antibody

Description of Dulaglutide Biosimilar - Anti-Glucagon-like peptide-1 receptor agonist mAb - Research Grade

General information about Dulaglutide

Dulaglutide is a novel glucagon-like peptide-1 agonist (GLP-1) biologic drug consisting of a dipeptidyl peptidase-IV-protected GLP-1 analogue covalently linked to a human IgG4-Fc heavy chain by a small peptide linker. Dulaglutide is indicated in the treatment of type 2 diabetes and can be used once a week. This product is for research use only.

Datasheet Download
MSDS Download

SDS-PAGE for Dulaglutide Biosimilar - Anti-Glucagon-like peptide-1 receptor agonist mAb

Dulaglutide Biosimilar - Anti-Glucagon-like peptide-1 receptor agonist mAb, on SDS-PAGE under non-reducing condition. The gel was stained overnight with Coomassie Blue. The purity of the antibody is greater than 95%.

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