Anti-Human CTLA-4 (Ipilimumab)

Cat# LT1600-1

Size : 1mg

Brand : Leinco Technologies

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AntiHuman CTLA4 (Ipilimumab)

Product No.: LT1600

Product No.LT1600
Clone
MDX010
Target
CTLA4
Product Type
Biosimilar Recombinant Human Monoclonal Antibody
Alternate Names
CD; GSE; GRD4; ALPS5; CD152; CTLA4; IDDM12; CELIAC3
Isotype
Human IgG1κ
Applications
B
,
CyTOF®
,
ELISA
,
FC

Antibody Details

Product Details

Reactive Species
Human
Host Species
Human
Expression Host
HEK293 Cells
FC Effector Activity
Active
Immunogen
Human CTLA4
Product Concentration
≥ 5.0 mg/ml
Endotoxin Level
< 1.0 EU/mg as determined by the LAL method
Purity
≥95% by SDS Page
≥95% monomer by analytical SEC
Formulation
This biosimilar antibody is aseptically packaged and formulated in 0.01 M phosphate buffered saline (150 mM NaCl) PBS pH 7.2 7.4 with no carrier protein, potassium, calcium or preservatives added. Due to inherent biochemical properties of antibodies, certain products may be prone to precipitation over time. Precipitation may be removed by aseptic centrifugation and/or filtration.
Product Preparation
Recombinant biosimilar antibodies are manufactured in an animal free facility using only in vitro protein free cell culture techniques and are purified by a multistep process including the use of protein A or G to assure extremely low levels of endotoxins, leachable protein A or aggregates.
Pathogen Testing
To protect mouse colonies from infection by pathogens and to assure that experimental preclinical data is not affected by such pathogens, all of Leinco’s recombinant biosimilar antibodies are tested and guaranteed to be negative for all pathogens in the IDEXX IMPACT I Mouse Profile.
Storage and Handling
Functional grade preclinical antibodies may be stored sterile as received at 28°C for up to one month. For longer term storage, aseptically aliquot in working volumes without diluting and store at ≤ 70°C. Avoid Repeated Freeze Thaw Cycles.
Regulatory Status
Research Use Only (RUO). NonTherapeutic.
Country of Origin
USA
Shipping
28°C Wet Ice
Applications and Recommended Usage?
Quality Tested by Leinco
FC The suggested concentration for Ipilimumab biosimilar antibody for staining cells in flow cytometry is ≤ 0.25 μg per 106 cells in a volume of 100 μl. Titration of the reagent is recommended for optimal performance for each application.
Additional Applications Reported In Literature ?
B
ELISA
CyTOF®
Each investigator should determine their own optimal working dilution for specific applications. See directions on lot specific datasheets, as information may periodically change.

Description

Description

Specificity
This nontherapeutic biosimilar antibody uses the same variable region sequence as the therapeutic antibody Ipilimumab. Ipilimumab binds to Human CTLA4. This product is for research use only.
Background
Cytotoxic Tlymphocyte–associated antigen 4 (CTLA4) is a protein receptor that serves as an immune checkpoint and downregulates the immune system. CTLA4 is constitutively expressed in regulatory T cells but is only upregulated in conventional T cells following activation. Many cancers, including Melanoma, are associated with CTLA4 upregulation because the body’s ability to recognize and destroy cancer cells is hampered by an inhibitory mechanism. Ipilimumab targets CTLA4 and works by turning off this inhibitory mechanism and, thus, enhances the body’s own immune response against cancer cells.”2 Emerging research suggests that combined blockade of PD1 and CTLA4, with Nivolumab and Ipilimumab respectively, could produce greater antitumor activity than blockade of either pathway alone.1 This costeffective, researchgrade AntiHuman CTLA4 (Ipilimumab) utilizes the same variable regions from the therapeutic antibody Ipilimumab making it ideal for research projects.
Antigen Distribution
CTLA4 is constitutively expressed in regulatory T cells.
PubMed
NCBI Gene Bank ID
Research Area
Biosimilars
.
Immunology

References & Citations

1. Wolchok, JD. et al. (2013) N Engl J Med 369(2):12233.
2. Soo, RA. et al. (2017) Lancet Oncol. 18(12):e731e741.
3. Lipson, EJ. and Drake, CG. (2011) Clin Cancer Res 17(22):695862.

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