Knockdown (KD) - Validated Primary Antibodies

Western blotting analysis using anti-APBB1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-APBB1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-phospho-CDC6 (Ser106) antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-phospho-CDC6 (Ser106) antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-NaQ™ ECL Substrate Kit .

Western blotting analysis using anti-Prolyl endopeptidase like antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Prolyl endopeptidase like antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Brain derived neurotrophic factor antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Brain derived neurotrophic factor antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Syntaxin binding protein 1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Syntaxin binding protein 1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Vinculin antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Vinculin antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Mitogen-activated protein kinase 1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Mitogen-activated protein kinase 1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-phospho-eIF2 alpha (Ser51) antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-phospho-eIF2 alpha (Ser51) antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-serpin family E member 1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-serpin family E member 1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-14-3-3 gamma antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-14-3-3 gamma antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-ABCG2 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-ABCG2 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-ACADVL antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-ACADVL antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-ACAP2 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-ACAP2 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit . ACAP2, ArfGAP with coiled-coil, ankyrin repeat and PH domains 2.

Western blotting analysis using anti-ACBD3 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-ACBD3 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Acetyl-CoA acetyltransferase 1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Acetyl-CoA acetyltransferase 1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Acetyl-CoA acyltransferase 2 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Acetyl-CoA acyltransferase 2 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Acetyl-CoA carboxylase alpha antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Acetyl-CoA carboxylase alpha antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Aconitase 2 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Aconitase 2 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-ACSL4 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-ACSL4 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit . ACSL4, acyl-CoA synthetase long chain family member 4.

Western blotting analysis using anti-Actin like 6A antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Actin like 6A antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Adiponectin receptor 1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Adiponectin receptor 1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-ADP ribosylation factor 1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-ADP ribosylation factor 1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-ADP ribosylation factor 5 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-ADP ribosylation factor 5 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-AGO3 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-AGO3 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-A-kinase anchoring protein 8 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-A-kinase anchoring protein 8 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-AKR1C1/AKR1C2 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-AKR1C1/AKR1C2 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Alkaline phosphatase antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Alkaline phosphatase antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-alpha smooth muscle Actin antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-alpha smooth muscle Actin antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-alpha smooth muscle Actin antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-alpha smooth muscle Actin1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-ALPP antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-ALPP antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-NaQ™ ECL Substrate Kit .

Western blotting analysis using anti-AMPK alpha 1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-AMPK alpha 1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Amyloid beta precursor like protein 2 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Amyloid beta precursor like protein 2 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Amyloid beta precursor protein antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Amyloid beta precursor protein antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Androgen receptor antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Androgen receptor antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Annexin A10 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Annexin A10 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Annexin A7 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Annexin A7 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Annexin V antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Annexin V antibody and HRP-conjugated goat anti rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-ANP32B antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-ANP32B antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit . ANP32B, acidic nuclear phosphoprotein 32 family member B.

Western blotting analysis using anti-AP1G1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-AP1G1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-AP2S1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-AP2S1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit . AP2S1, adaptor related protein complex 2 subunit sigma 1.

Western blotting analysis using anti-AP2S1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-AP2S1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-APPL1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-APPL1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit . APPL1, adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 1.

Western blotting analysis using anti-Aquaporin 1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Aquaporin 1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Arg2 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Arg2 antibody and HRP-conjugated goat anti rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-arginyltransferase 1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-arginyltransferase 1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-NaQ™ ECL Substrate Kit .

Western blotting analysis using anti-Argonaute RISC catalytic component 2 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Argonaute RISC catalytic component 2 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-ARID1A antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-ARID1A antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Arp2 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Arp2 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Arp3 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Arp3 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .

Western blotting analysis using anti-Arrestin beta 1 antibody . Total cell lysates (30 μg) from various cell lines were loaded and separated by SDS-PAGE. The blot was incubated with anti-Arrestin beta 1 antibody and HRP-conjugated goat anti-rabbit secondary antibody respectively. Image was developed using anti-FeQ™ ECL Substrate Kit .