Antibody data
- Antibody Data
- Antigen structure
- References [4]
- Comments [0]
- Validations [0]
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Validation data
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- Product number
- 66282-1-Ig - Provider product page
- Provider
- Proteintech Group
- Product name
- CD200 antibody
- Antibody type
- Monoclonal
- Description
- KD/KO validated CD200 antibody (Cat. #66282-1-Ig) is a mouse monoclonal antibody that shows reactivity with human and has been validated for the following applications: FC, IHC, WB,ELISA.
- Reactivity
- Human
- Host
- Mouse
- Conjugate
- Unconjugated
- Isotype
- IgG
- Antibody clone number
- 5F3D6
- Vial size
- 20ul, 150ul
Submitted references Inflammatory dendritic cells restrain CD11b(+)CD4(+) CTLs via CD200R in human NSCLC.
Multiplex Quantitative Analysis of Tumor-Infiltrating Lymphocytes, Cancer-Associated Fibroblasts, and CD200 in Pancreatic Cancer.
CD200 and CD200R1 are differentially expressed and have differential prognostic roles in non-small cell lung cancer.
CD200-positive cancer associated fibroblasts augment the sensitivity of Epidermal Growth Factor Receptor mutation-positive lung adenocarcinomas to EGFR Tyrosine kinase inhibitors.
Lin M, Chen D, Shao Z, Liu Q, Hao Z, Xin Z, Chen Y, Wu W, Chen X, He T, Wu D, Wu P
Cell reports 2024 Feb 27;43(2):113767
Cell reports 2024 Feb 27;43(2):113767
Multiplex Quantitative Analysis of Tumor-Infiltrating Lymphocytes, Cancer-Associated Fibroblasts, and CD200 in Pancreatic Cancer.
MacNeil T, Vathiotis IA, Shafi S, Aung TN, Zugazagoitia J, Gruver AM, Driscoll K, Rimm DL
Cancers 2021 Nov 2;13(21)
Cancers 2021 Nov 2;13(21)
CD200 and CD200R1 are differentially expressed and have differential prognostic roles in non-small cell lung cancer.
Yoshimura K, Suzuki Y, Inoue Y, Tsuchiya K, Karayama M, Iwashita Y, Kahyo T, Kawase A, Tanahashi M, Ogawa H, Inui N, Funai K, Shinmura K, Niwa H, Sugimura H, Suda T
Oncoimmunology 2020;9(1):1746554
Oncoimmunology 2020;9(1):1746554
CD200-positive cancer associated fibroblasts augment the sensitivity of Epidermal Growth Factor Receptor mutation-positive lung adenocarcinomas to EGFR Tyrosine kinase inhibitors.
Ishibashi M, Neri S, Hashimoto H, Miyashita T, Yoshida T, Nakamura Y, Udagawa H, Kirita K, Matsumoto S, Umemura S, Yoh K, Niho S, Tsuboi M, Masutomi K, Goto K, Ochiai A, Ishii G
Scientific reports 2017 Apr 21;7:46662
Scientific reports 2017 Apr 21;7:46662
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