Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-400 |
Flow Cytometry (Fixed): | 1:50-200 |
(Boiling the paraffin sections in 10mM citrate buffer,pH6.0,or PH8.0 EDTA repair liquid for 20 mins is required for the staining of formalin/paraffin sections.) Optimal working dilutions must be determined by end user. |
Figure 1. Western blot analysis of anti-ATP citrate lyase antibody (M02372-1). The sample well of each lane was loaded with 50ug of sample under reducing conditions.
Lane 1: Human placenta tissue lysates,
Lane 2: U-87MG whole cell lysates,
Lane 3: HEK293 whole cell lysates,
Lane 4: Caco-2 whole cell lysates,
Lane 5: HL-60 whole cell lysates,
Lane 6: Raji whole cell lysates,
Lane 7: THP-1 whole cell lysates,
Lane 8: PANC-1 whole cell lysates,Use mouse Anti-ATP citrate lyase 1:1000, probed with a goat anti-mouse IgG-HRP secondary antibody. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1001). A specific band was detected for ATP citrate lyase at approximately 127KD. The expected band size for ATP citrate lyase is at 121KD.
Figure 2. Western blot analysis of anti-ATP citrate lyase antibody (M02372-1). The sample well of each lane was loaded with 50ug of sample under reducing conditions.
Lane 1: Rat lung tissue lysates,
Lane 2: Rat testicular tissue lysates,
Lane 3: Rat kidney tissue lysates,
Lane 4: Rat brain tissue lysates,
Lane 5: Mouse lung tissue lysates,
Lane 6: Mouse testicular tissue lysates,
Lane 7: Mouse kidney tissue lysates,Use mouse Anti-ATP citrate lyase 1:1000, probed with a goat anti-mouse IgG-HRP secondary antibody. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1001). A specific band was detected for ATP citrate lyase at approximately 127KD. The expected band size for ATP citrate lyase is at 121KD.
Figure 3. IHC analysis using Anti-ATP citrate lyase antibody (M02372-1) detected in paraffin-embedded section of human pancreatic cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB as the chromogen.
Figure 4. IHC analysis using Anti-ATP citrate lyase antibody (M02372-1) detected in paraffin-embedded section of human testis cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB as the chromogen.
Figure 5. IHC analysis using Anti-ATP citrate lyase antibody (M02372-1) detected in paraffin-embedded section of mouse pancreas tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB as the chromogen.
Figure 6. IHC analysis using Anti-ATP citrate lyase antibody (M02372-1) detected in paraffin-embedded section of rat pancreas tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB as the chromogen.
Figure 7. Flow cytometry analysis of A549 cell(1:100) DyLight 488 conjugated goat anti-mouse IgG(blue) was used as secondary antibody. Isotype control antibody (Green line) was mouse IgG DyLight 488. Unlabelled sample (Red line).
Figure 8. ICC analysis using anti-ATP citrate lyase antibody (M02372-1) was detected in immersion fixed MCF-7 cell line . Cells were stained using the Dylight488-conjugated Anti-mouse IgG Secondary Antibody (green)(Catalog#BA1127) and counterstained with DAPI (blue).
Figure 1. Western blot analysis of anti-ATP citrate lyase antibody (M02372-1). The sample well of each lane was loaded with 50ug of sample under reducing conditions.
Lane 1: Human placenta tissue lysates,
Lane 2: U-87MG whole cell lysates,
Lane 3: HEK293 whole cell lysates,
Lane 4: Caco-2 whole cell lysates,
Lane 5: HL-60 whole cell lysates,
Lane 6: Raji whole cell lysates,
Lane 7: THP-1 whole cell lysates,
Lane 8: PANC-1 whole cell lysates,Use mouse Anti-ATP citrate lyase 1:1000, probed with a goat anti-mouse IgG-HRP secondary antibody. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1001). A specific band was detected for ATP citrate lyase at approximately 127KD. The expected band size for ATP citrate lyase is at 121KD.
Figure 2. Western blot analysis of anti-ATP citrate lyase antibody (M02372-1). The sample well of each lane was loaded with 50ug of sample under reducing conditions.
Lane 1: Rat lung tissue lysates,
Lane 2: Rat testicular tissue lysates,
Lane 3: Rat kidney tissue lysates,
Lane 4: Rat brain tissue lysates,
Lane 5: Mouse lung tissue lysates,
Lane 6: Mouse testicular tissue lysates,
Lane 7: Mouse kidney tissue lysates,Use mouse Anti-ATP citrate lyase 1:1000, probed with a goat anti-mouse IgG-HRP secondary antibody. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1001). A specific band was detected for ATP citrate lyase at approximately 127KD. The expected band size for ATP citrate lyase is at 121KD.
Figure 3. IHC analysis using Anti-ATP citrate lyase antibody (M02372-1) detected in paraffin-embedded section of human pancreatic cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB as the chromogen.
Figure 4. IHC analysis using Anti-ATP citrate lyase antibody (M02372-1) detected in paraffin-embedded section of human testis cancer tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB as the chromogen.
Figure 5. IHC analysis using Anti-ATP citrate lyase antibody (M02372-1) detected in paraffin-embedded section of mouse pancreas tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB as the chromogen.
Figure 6. IHC analysis using Anti-ATP citrate lyase antibody (M02372-1) detected in paraffin-embedded section of rat pancreas tissue. Biotinylated goat anti-mouse IgG was used as secondary antibody. The tissue section was developed using Strepavidin-Biotin-Complex (SABC) (Catalog # SA1021) with DAB as the chromogen.
Figure 7. Flow cytometry analysis of A549 cell(1:100) DyLight 488 conjugated goat anti-mouse IgG(blue) was used as secondary antibody. Isotype control antibody (Green line) was mouse IgG DyLight 488. Unlabelled sample (Red line).
Figure 8. ICC analysis using anti-ATP citrate lyase antibody (M02372-1) was detected in immersion fixed MCF-7 cell line . Cells were stained using the Dylight488-conjugated Anti-mouse IgG Secondary Antibody (green)(Catalog#BA1127) and counterstained with DAPI (blue).