Anti-AADACL1/NCEH1 Antibody

筛选器： All WB FCM ELISA

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  Figure 1. Western blot analysis of anti-AADACL1/NCEH1 antibody (A06478-1). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
  Lane 1: human A431 whole cell lysates,
  Lane 2: human PC-3 whole cell lysates,
  Lane 3: human SIHA whole cell lysates,
  Lane 4: human A549 whole cell lysates.
  After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-AADACL1/NCEH1 antigen affinity purified polyclonal antibody (A06478-1) and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for AADACL1/NCEH1 at approximately 46 kDa. The expected band size for AADACL1/NCEH1 is at 46,55 kDa.

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  Figure 2. Flow Cytometry analysis of HepG2 cells using anti-AADACL1/NCEH1 antibody (A06478-1).
  Overlay histogram showing HepG2 cells stained with A06478-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-AADACL1/NCEH1 Antibody (A06478-1, 1:100). DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 1:100) was used as secondary antibody. Isotype control antibody (Green line) was rabbit IgG (Catalog # BA1045) (1:100) used under the same conditions. Unlabelled sample (Red line) was also used as a control.

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  Figure 1. Western blot analysis of anti-AADACL1/NCEH1 antibody (A06478-1). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
  Lane 1: human A431 whole cell lysates,
  Lane 2: human PC-3 whole cell lysates,
  Lane 3: human SIHA whole cell lysates,
  Lane 4: human A549 whole cell lysates.
  After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-AADACL1/NCEH1 antigen affinity purified polyclonal antibody (A06478-1) and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for AADACL1/NCEH1 at approximately 46 kDa. The expected band size for AADACL1/NCEH1 is at 46,55 kDa.

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  Figure 2. Flow Cytometry analysis of HepG2 cells using anti-AADACL1/NCEH1 antibody (A06478-1).
  Overlay histogram showing HepG2 cells stained with A06478-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-AADACL1/NCEH1 Antibody (A06478-1, 1:100). DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 1:100) was used as secondary antibody. Isotype control antibody (Green line) was rabbit IgG (Catalog # BA1045) (1:100) used under the same conditions. Unlabelled sample (Red line) was also used as a control.

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