Human CD19 (20-291), Fc Tag, low endotoxin (CD9-H5259) is expressed from human 293 cells (HEK293). It contains AA Pro 20 - Lys 291 (Accession # AAH06338).
Predicted N-terminus: Pro 20
This protein carries a human IgG1 Fc tag at the C-terminus.
The protein has a calculated MW of 56.3 kDa. The protein migrates as 56-66 kDa under reducing (R) condition (SDS-PAGE) due to glycosylation.
Less than 0.1 EU per μg by the LAL method.
>95% as determined by SDS-PAGE.
Lyophilized from 0.22 μm filtered solution in PBS, pH7.4. Normally trehalose is added as protectant before lyophilization.
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Please see Certificate of Analysis for specific instructions.
For best performance, we strongly recommend you to follow the reconstitution protocol provided in the CoA.
For long term storage, the product should be stored at lyophilized state at -20°C or lower.
Please avoid repeated freeze-thaw cycles.
No activity loss was observed after storage at:
- 4-8°C for 12 months in lyophilized state;
- -70°C for 3 months under sterile conditions after reconstitution.
Human CD19 (20-291), Fc Tag, low endotoxin on SDS-PAGE under reducing (R) condition. The gel was stained overnight with Coomassie Blue. The purity of the protein is greater than 95%.
Immobilized FMC63 at 1 μg/mL (100 μL/well) can bind Human CD19 (20-291), Fc Tag, low endotoxin (Cat. No. CD9-H5259) with a linear range of 0.039-0.625 μg/mL (QC tested).
CAR阳性表达率检测（Evaluation of CAR expression ）
FACS Analysis of anti-CD19 CAR Expression
293 cells were transfected with FCM63-scFv and RFP tag. 2x105 of the cells were first incubated with A. Human Fc tag control. B. Recombinant human CD19, Fc Tag, low endotoxin (Cat. No. CD9-H5259, 10 μg/ml ). C. Recombinant human CD19, Fc Tag, low endotoxin (Cat. No. CD9-H5259, 10 μg/ml ) and FMC63 (Mouse anti-CD19 antibody). The FITC anti-human IgG Fc was used to analyse with FACS. RFP was used to evaluate CAR (FMC63-scFv) expression and FITC was used to evaluate the binding activity of recombinant human CD19, Fc Tag, low endotoxin.
FACS Analysis of anti-CD19 CAR Expression
Human T cells were lentivirally transduced with anti-CD19 CAR and cultured for 3 days. Three days post-transduction, 1e6 cells were first incubated with 100 ul Human CD19 Protein, Fc Tag, low endotoxin (Cat. No. CD9-H5259, 10 μg/ml), washed and then stained with PE anti-human IgG Fc Antibody. Non-transduced T cells were used as a control for gating of CAR expression. (Data are kindly provided by XIAMEN Anti-hela Biological TechnologyTrade Co. Ltd.)
Authors: Hsu H, et al.
Journal: J Immunol
Application: Granule mobilization assay
Authors: De Oliveira SN, et al.
Journal: J Transl Med 2013
Application: Flow cytometry
B-lymphocyte antigen CD19 is also known as CD19 (Cluster of Differentiation 19), is a single-pass type I membrane protein which contains two Ig-like C2-type (immunoglobulin-like) domains. CD19 is expressed on follicular dendritic cells and B cells. In fact, it is present on B cells from earliest recognizable B-lineage cells during development to B-cell blasts but is lost on maturation to plasma cells. It primarily acts as a B cell co-receptor in conjunction with CD21 and CD81. Upon activation, the cytoplasmic tail of CD19 becomes phosphorylated, which leads to binding by Src-family kinases and recruitment of PI-3 kinase. As on T cells, several surface molecules form the antigen receptor and form a complex on B lymphocytes. The (almost) B cell-specific CD19 phosphoglycoprotein is one of these molecules. The others are CD21 and CD81. These surface immunoglobulin (sIg)-associated molecules facilitate signal transduction. On living B cells, anti-immunoglobulin antibody mimicking exogenous antigen causes CD19 to bind to sIg and internalize with it. The reverse process has not been demonstrated, suggesting that formation of this receptor complex is antigen-induced. This molecular association has been confirmed by chemical studies. Mutations in CD19 are associated with severe immunodeficiency syndromes characterized by diminished antibody production. CD19 has been shown to interact with: CD81, CD82, Complement receptor 2, and VAV2.