1. Immunology/Inflammation
  2. PD-1/PD-L1
  3. Sintilimab

Sintilimab  (Synonyms: IBI308)

製品番号: HY-P99048 純度: 99.1%
COA Technical Support

Sintilimab (IBI308) is a safe and effectivel humanized IgG4 monoclonal antibody that binds to PD-1 with a KD value of 74 pM. Sintilimab blocks the interaction of PD-1 with its ligands (PD-L1 and PL-L2), consequently helping to restore the endogenous antitumour T-cell response. Sintilimab combined with prebiotics inhibits tumor volume and regulates immune cell subpopulation balance in lung adenocarcinoma mice. Sintilimab can be used for the research of classical Hodgkin's lymphoma, non-small cell lung cancer and oesophageal cancer.

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CAS 番号 : 2072873-06-2

容量 価格(税別) 在庫状況 数量
>無料サンプル (100 μg)   今すぐ申し込む  
1 mg $200 在庫あり
5 mg $520 在庫あり
10 mg $885 在庫あり
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100 mg   お問い合わせ  

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製品説明

Sintilimab (IBI308) is a safe and effectivel humanized IgG4 monoclonal antibody that binds to PD-1 with a KD value of 74 pM. Sintilimab blocks the interaction of PD-1 with its ligands (PD-L1 and PL-L2), consequently helping to restore the endogenous antitumour T-cell response. Sintilimab combined with prebiotics inhibits tumor volume and regulates immune cell subpopulation balance in lung adenocarcinoma mice. Sintilimab can be used for the research of classical Hodgkin's lymphoma, non-small cell lung cancer and oesophageal cancer[1][2][3][4][5].

Isotype

Human IgG4 kappa

Recommend Isotype Controls
Species Reactivity

Human

IC50 & Target

PDCD1/PD-1/CD279

体外実験

Sintilimab (12 h) shows a high level of PD-1 occupancy and has superior T cell activating characteristics in human peripheral blood mononuclear cells (PBMCs)[2].
Sintilimab (0.16-100 nM; 5 days) induces high secretion levels of IFN-γ and IL-2 in primary T cell assays[6].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

体内実験

Sintilimab (0.1 mg/kg, 1 mg/kg and 10 mg/kg, i.p., a single dose for 1, 8, 12, 15 days) shows antitumor effects against NCI-H292 tumors in a humanized mouse model[2].
Sintilimab (1 mg/kg, 3 mg/kg and 10 mg/kg, s.c., a single dose) demonstrates a high affinity for PD-1 molecules in NCI-H292 tumor-bearing NOG mice[2].
Sintilimab (20 mg/kg, i.p., once interval 2 days for 21 days) combined with prebiotics inhibits the volume of transplanted tumors in lung adenocarcinoma and alleviates the liver and kidney injury[4].

Pharmacokinetic parameters of Sintilimab (10 mg/kg, i.v., a single dose) in hPD-1 knock-in mouse[2]

Parameter AUC0-4 (h·μg/mL) AUCinf (h·μg/mL) CL (mL/h) Cmax (μg/mL) T1/2 (h) Vss (mL)
Sintilimab 6597.888 7846.554 0.025 218.519 35.623 1.262

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: NOG mice reconstituted with human PBMCs[2]
Dosage: 1 mg/kg, 3 mg/kg and 10 mg/kg
Administration: i.p., a single dose at 24 h and 72 h
Result: Dose-dependently showed a higher percentage of PD-1 molecule occupancy compared with MDX-1106 (HY-P9903) and MK-3475 (HY-P9902) in mice.
Animal Model: NCI-H292 tumor-bearing NOG mice[2]
Dosage: 1 mg/kg, 3 mg/kg and 10 mg/kg
Administration: s.c., a single dose at 24 h
Result: Increased PD-1 receptor occupancy in both peripheral and CD3+ tumor-infiltrating T cells (TILs) to more than 90% in NCI-H292 tumor-bearing mice.
Animal Model: NCI-H292 tumors in a humanized xenograft mouse model[2]
Dosage: 0.1 mg/kg, 1 mg/kg and 10 mg/kg
Administration: i.p., a single dose at day 1, 8, 12, 15
Result: Inhibited tumor growth much more effectively and was significantly higher in the ratio of CD8+ to Treg tumor-infiltrating lymphocytes than MDX-1106 (HY-P9903) and MK-3475 (HY-P9902) in mice.
Animal Model: C57BL/6J mice (6-8 weeks old, body mass 20-25 g) with lung adenocarcinoma[4]
Dosage: 20 mg/kg
Administration: i.p., once interval 2 days for 21 days
Result: Significantly decreased the tumor volume, showed blurred cell structure and mildly damaged liver lobules and reduced liver and kidney injury in lung adenocarcinoma mice.
臨床実験
Gene ID

5133  [NCBI]

Accession
Application

ELISA, FACS, Functional assay

Conjugated

Unconjugated

Reconsititution

The product can be reconstituted/diluted with sterile PBS or saline.

分子量

144.04 kDa

CAS 番号
Appearance

Liquid

Color

Colorless to light yellow

SMILES

[Sintilimab]

Formulation

Please refer to the lot-specific COA for specific buffer information.

保管条件

Please store the product under the recommended conditions in the Certificate of Analysis.

Format
  • Human IgG4 kappa
Biological Activity
  • Immobilized PD-1 Protein, Human (143a.a, HEK293, His, HY-P7396) can bind Sintilimab. The EC50 for this effect is 6.653 ng/mL.
  • Flow cytometric analysis of 1X106 10 ng/mL PMA and 1 μg/mL Ionomycin co-stimulated Jurkat cells(24h) labeling Sintilimab (HY-P99048, red). Cells were fixed with 4% paraformaldehyde. Then stained with the primary antibody at 1/200 dilution for an hour at 4℃. Alexa Fluor 488-conjugated AffiniPure Goat Anti-Human IgG H&L (HY-P83776) was used as the secondary antibody at 1/1,000 dilution for 30 minutes at 4℃. Human IgG4 kappa (HY-P99003, blue) was used as the isotype control, cells without incubation with primary antibody were used as the unlabeled control (black).
純度とドキュメンテーション

純度: 99.1%

参考文献
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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製品名:
Sintilimab
製品番号:
HY-P99048
数量:
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