NeuroMab™ Anti-HRG Beta 1 Antibody (NRP-0422-P1901)
Functional antibody against Human NRG1
- Host Species:
- Chimeric
- Species Reactivity:
- Human
- Applications:
- FC; ELISA; In Vitro; Inhib; In Vivo
To download a Certificate of Analysis, please enter a lot number in the search box below. Note: Certificate of Analysis not available for kit components.
Lot Number
SPECIFIC INQUIRY
inquiryDescription
Species Reactivity
Clonality
Host Species
Applications
Formulation
Preservatives
Concentration
Purification
Purity
Endotoxin Level
Low Endotoxin < 1 EU/mg
Shipping
Storage
Research Use Only
Target
Official Name
Full Name
Alternative Names
Figure 1 Points illustrating the results of flow cytometry analysis of the degree of binding of antibodies against human NRG1 protein (8a2, 8a4, 10bM3, and 10b2M3) to cell lines (NRG1-α/st293T or NRG1-) picture. b/st293T) stably expresses at a high level either of the human NRG1-α protein and the human NRG1-β1 protein with an HA tag added to its N-terminus.
Figure 3 is a dot graph for illustrating the results of analyzing the degree of binding of 10bM3 and 10b2M3 to a cell line stably expressing a (NRG1-α/st293T, NRG1-b/st293T or NRG1-b2/st293T) by flow cytometry. High levels of any of human NRG1-α protein, human NRG1-β1 protein, and human NRG1-β2 protein with an HA tag added to the N-terminus.
Figure 4 is a graph illustrating the results of ELISA analysis of the degree of binding of the antibodies (8a4, 10bM3, 10b2M3) to factors belonging to the EGF family (EGF, HB-EGF, TGFα (TGFα)). , AREG, NRG1-α (NRG1-α) and NRG1-b (NRG1-β1)).
Figure 5 is a graph illustrating the results of analysis by flow cytometry of 8a2 and the antibodies (8a4, 10bM3, and 10b2M3) for inhibiting cleavage of human NRG1-α protein, which would otherwise be cleaved by PMA.
Figure 6 is a graph illustrating the results of analysis by flow cytometry of 8a2 and the antibodies (8a4, 10bM3 and 10b2M3) for inhibition of human NRG1-β1 protein cleavage, which would otherwise occur in PMA.
Figure 7 is a photograph illustrating the results of Western blot analysis of the activity of 8a2 and the antibodies (8a4, 10bM3, 10b2M3) to inhibit human NRG1-α protein-induced ErbB3 phosphorylation.
Figure 8 is a dot diagram illustrating the results of flow cytometry analysis of the degree of binding of the chimeric antibodies (ch-8a4, ch-10bM3, ch-10b2M3) to NRG1-α/st293T and NRG1-b. /st293T, or NRG1-b2/st293T.
Figure 9 is a graph illustrating time-dependent changes in tumor volume in xenografted mice administered the antibody (10b2M3 or ch-10b2M3).
Figure 2 is used to illustrate the analysis of antibodies by ELISA with partial-length human NRG1-α proteins (ag4a to ag13a and agPa) and partial-length human NRG1-β1 proteins (ag4b to ag13b, ag4b to ag13b, and Pb).
Publications (0)