Western Blot using CPTC-Gelsolin-1 as primary Ab against Ag 10594 (lane 2). Also included are molecular wt. standards (lane 1) and mouse IgG control (lane 3).
Indirect ELISA (ie, binding of Antibody to Antigen coated plate)
Protein Array in which CPTC-Gelsolin-1 CPTC-AKR1B1-1 is screened against the NCI60 cell line panel for expression. Data is normalized to a mean signal of 1.0 and standard deviation of 0.5. Color conveys over-expression level (green), basal level (blue), under-expression level (red).
Western Blot using CPTC-Gelsolin-2 as primary Ab against Gelsolin (rAg 10594) in lane 2. Also included are molecular wt. standards (lane 1) and mouse IgG control (lane 3).
Western Blot using CPTC-Gelsolin-2 as primary Ab against cell lysate from transiently overexpressed HEK293T cells form Origene (lane 3). Also included are molecular wt. standards (lane 1), lysate from non-transfected HEK293T cells as neg control (lane 4) and recombinant Ag Gelsolin (NCI 10594) in (lane 2).
Indirect ELISA (ie, binding of Antibody to Antigen coated plate). Note: B50% represents the concentration of Ab required to generate 50% of maximum binding.
This antibody is not suitable for use in a Reverse Phase Protein Array format as described in SOP M-105.
This antibody is not suitable for use in an Immunohistochemistry format as described in SOP M-106.
This antibody is not suitable for use in an Immunohistochemistry format as described in SOP M-106.
This table summarizes the results of the pairing experiment with Gelsolin antibodies.
Kinetic titration data for Gelsolin-2 using Biacore SPR method
Western Blot using CPTC-Gelsolin-3 as primary Ab against Gelsolin (rAg 10594) in lane 2. Also included are molecular wt. standards (lane 1) and mouse IgG control (lane 3).
Western Blot using CPTC-Gelsolin-3 as primary Ab against cell lysate from transiently overexpressed HEK293T cells form Origene (lane 3). Also included are molecular wt. standards (lane 1), lysate from non-transfected HEK293T cells as neg control (lane 4) and recombinant Ag Gelsolin (NCI 10594) in (lane 2).
Indirect ELISA (ie, binding of Antibody to Antigen coated plate). Note: B50% represents the concentration of Ab required to generate 50% of maximum binding.
This antibody is not suitable for use in a Reverse Phase Protein Array format as described in SOP M-105.
This antibody is not suitable for use in an Immunohistochemistry format as described in SOP M-106.
This antibody is not suitable for use in an Immunohistochemistry format as described in SOP M-106.
This table summarizes the results of the pairing experiment with Gelsolin antibodies.
Kinetic titration data for Gelsolin-3 antibody using Biacore SPR method
Western Blot using CPTC-Gelsolin-4 as primary Ab against Gelsolin (rAg 10594) in lane 2. Also included are molecular wt. standards (lane 1) and mouse IgG control (lane 3).
Western Blot using CPTC-Gelsolin-4 as primary Ab against cell lysate from transiently overexpressed HEK293T cells form Origene (lane 3). Also included are molecular wt. standards (lane 1), lysate from non-transfected HEK293T cells as neg control (lane 4) and recombinant Ag Gelsolin (NCI 10594) in (lane 2).
Indirect ELISA (ie, binding of Antibody to Antigen coated plate). Note: B50% represents the concentration of Ab required to generate 50% of maximum binding.
This antibody is not suitable for use in a Reverse Phase Protein Array format as described in SOP M-105.
This antibody is not suitable for use in an Immunohistochemistry format as described in SOP M-106.
This antibody is not suitable for use in an Immunohistochemistry format as described in SOP M-106.
This table summarizes the results of the pairing experiment with Gelsolin antibodies.
Kinetic titration data for Gelsolin-4 antibody using Biacore SPR method
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