rabbit apoe antibody Search Results


anti apoe antibody  (Sino Biological)
90
Sino Biological anti apoe antibody
( a–c ) Concentrated culture supernatants from HCV persistently infected Huh7.5.1 cells treated with siRNAs were subjected to 20–60% sucrose gradients and equilibrium ultracentrifugation. Eleven fractions were harvested from the top of the sucrose gradients and used to determine the density, HCV RNA levels, infectivity titer, and HCV core amounts. ( a ) The buoyant density of sucrose was plotted with the HCV RNA level as measured by qRT-PCR in each fraction. ( b ) The HCV infectivity of each fraction was evaluated. ( c ) Left: Western blot analysis of the <t>ApoE</t> and core protein levels in each fraction of the sucrose gradient. The right panel displays the relative core-to-total-core amounts as detected in all fractions. ( d ) Western blot analysis of ApoE from the indicated fractions of the sucrose gradient those were rich in HCV infectious particles. ( e ) Western blot analysis of total supernatants ApoE (left) and cell lysates ApoE (right). ( f ) The effect <t>of</t> <t>CIDEB</t> silencing on the co-localization of NS5A-EGFP with endogenous ApoE in HCV- Jc1EGFP persistently infected Huh7.5.1 cells. The magnification of the frame section of merged images is presented at the right of the merged images. ( g ) The effect of CIDEB silencing on NS5A-ApoE and E2-ApoE co-localization was evaluated by overlap efficiency. ( h ) The effect of CIDEB silencing on the NS5A-ApoE interaction. Huh7.5.1 cells were transduced with Flag-NS5A and HA-ApoE lentivirus for 48 h and then treated with siNC or siCIDEB for 72 h. Cell lysates were subjected to IP with an anti-Flag antibody and then immunoblotted with an anti-HA antibody.
Anti Apoe Antibody, supplied by Sino Biological, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+apoe+antibody/APOE+%2F+apolipoprotein+E+Antibody%2C+Rabbit+PAb%2C+Antigen+Affinity+Purified/pmc04901263-155-53-56
Average 90 stars, based on 1 article reviews
anti apoe antibody - by Bioz Stars, 2026-09
90/100 stars
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apoe antibody (16h22l18), abfinity rabbit monoclonal  (Thermo Fisher)
N/A
APOE Monoclonal Antibody for Western Blot, IF, ICC
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rabbit polyclonal antibody anti apoe  (Sino Biological)
90
Sino Biological rabbit polyclonal antibody anti apoe
( a–c ) Concentrated culture supernatants from HCV persistently infected Huh7.5.1 cells treated with siRNAs were subjected to 20–60% sucrose gradients and equilibrium ultracentrifugation. Eleven fractions were harvested from the top of the sucrose gradients and used to determine the density, HCV RNA levels, infectivity titer, and HCV core amounts. ( a ) The buoyant density of sucrose was plotted with the HCV RNA level as measured by qRT-PCR in each fraction. ( b ) The HCV infectivity of each fraction was evaluated. ( c ) Left: Western blot analysis of the <t>ApoE</t> and core protein levels in each fraction of the sucrose gradient. The right panel displays the relative core-to-total-core amounts as detected in all fractions. ( d ) Western blot analysis of ApoE from the indicated fractions of the sucrose gradient those were rich in HCV infectious particles. ( e ) Western blot analysis of total supernatants ApoE (left) and cell lysates ApoE (right). ( f ) The effect <t>of</t> <t>CIDEB</t> silencing on the co-localization of NS5A-EGFP with endogenous ApoE in HCV- Jc1EGFP persistently infected Huh7.5.1 cells. The magnification of the frame section of merged images is presented at the right of the merged images. ( g ) The effect of CIDEB silencing on NS5A-ApoE and E2-ApoE co-localization was evaluated by overlap efficiency. ( h ) The effect of CIDEB silencing on the NS5A-ApoE interaction. Huh7.5.1 cells were transduced with Flag-NS5A and HA-ApoE lentivirus for 48 h and then treated with siNC or siCIDEB for 72 h. Cell lysates were subjected to IP with an anti-Flag antibody and then immunoblotted with an anti-HA antibody.
Rabbit Polyclonal Antibody Anti Apoe, supplied by Sino Biological, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+apoe+antibody/ApoE+%2F+Apolipoprotein+E+Antibody%2C+Rabbit+PAb/pmc03946557-53-0-7
Average 90 stars, based on 1 article reviews
rabbit polyclonal antibody anti apoe - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
rabbit anti-apoe antibody  (Bioworld Antibodies)
90
Bioworld Antibodies rabbit anti-apoe antibody
( a–c ) Concentrated culture supernatants from HCV persistently infected Huh7.5.1 cells treated with siRNAs were subjected to 20–60% sucrose gradients and equilibrium ultracentrifugation. Eleven fractions were harvested from the top of the sucrose gradients and used to determine the density, HCV RNA levels, infectivity titer, and HCV core amounts. ( a ) The buoyant density of sucrose was plotted with the HCV RNA level as measured by qRT-PCR in each fraction. ( b ) The HCV infectivity of each fraction was evaluated. ( c ) Left: Western blot analysis of the <t>ApoE</t> and core protein levels in each fraction of the sucrose gradient. The right panel displays the relative core-to-total-core amounts as detected in all fractions. ( d ) Western blot analysis of ApoE from the indicated fractions of the sucrose gradient those were rich in HCV infectious particles. ( e ) Western blot analysis of total supernatants ApoE (left) and cell lysates ApoE (right). ( f ) The effect <t>of</t> <t>CIDEB</t> silencing on the co-localization of NS5A-EGFP with endogenous ApoE in HCV- Jc1EGFP persistently infected Huh7.5.1 cells. The magnification of the frame section of merged images is presented at the right of the merged images. ( g ) The effect of CIDEB silencing on NS5A-ApoE and E2-ApoE co-localization was evaluated by overlap efficiency. ( h ) The effect of CIDEB silencing on the NS5A-ApoE interaction. Huh7.5.1 cells were transduced with Flag-NS5A and HA-ApoE lentivirus for 48 h and then treated with siNC or siCIDEB for 72 h. Cell lysates were subjected to IP with an anti-Flag antibody and then immunoblotted with an anti-HA antibody.
Rabbit Anti Apoe Antibody, supplied by Bioworld Antibodies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+apoe+antibody/rabbit+anti+apoe+antibody/pm28241308-91-12-17
Average 90 stars, based on 1 article reviews
rabbit anti-apoe antibody - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
anti-canine apoe rabbit polyclonal antibody  (Cloud-Clone corp)
90
Cloud-Clone corp anti-canine apoe rabbit polyclonal antibody
( a–c ) Concentrated culture supernatants from HCV persistently infected Huh7.5.1 cells treated with siRNAs were subjected to 20–60% sucrose gradients and equilibrium ultracentrifugation. Eleven fractions were harvested from the top of the sucrose gradients and used to determine the density, HCV RNA levels, infectivity titer, and HCV core amounts. ( a ) The buoyant density of sucrose was plotted with the HCV RNA level as measured by qRT-PCR in each fraction. ( b ) The HCV infectivity of each fraction was evaluated. ( c ) Left: Western blot analysis of the <t>ApoE</t> and core protein levels in each fraction of the sucrose gradient. The right panel displays the relative core-to-total-core amounts as detected in all fractions. ( d ) Western blot analysis of ApoE from the indicated fractions of the sucrose gradient those were rich in HCV infectious particles. ( e ) Western blot analysis of total supernatants ApoE (left) and cell lysates ApoE (right). ( f ) The effect <t>of</t> <t>CIDEB</t> silencing on the co-localization of NS5A-EGFP with endogenous ApoE in HCV- Jc1EGFP persistently infected Huh7.5.1 cells. The magnification of the frame section of merged images is presented at the right of the merged images. ( g ) The effect of CIDEB silencing on NS5A-ApoE and E2-ApoE co-localization was evaluated by overlap efficiency. ( h ) The effect of CIDEB silencing on the NS5A-ApoE interaction. Huh7.5.1 cells were transduced with Flag-NS5A and HA-ApoE lentivirus for 48 h and then treated with siNC or siCIDEB for 72 h. Cell lysates were subjected to IP with an anti-Flag antibody and then immunoblotted with an anti-HA antibody.
Anti Canine Apoe Rabbit Polyclonal Antibody, supplied by Cloud-Clone corp, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+apoe+antibody/anti+canine+apoe+rabbit+polyclonal+antibody/pm32880234-21-26-32
Average 90 stars, based on 1 article reviews
anti-canine apoe rabbit polyclonal antibody - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
anti-rabbit apoe antibody 381129  (ZenBio)
90
ZenBio anti-rabbit apoe antibody 381129
( a–c ) Concentrated culture supernatants from HCV persistently infected Huh7.5.1 cells treated with siRNAs were subjected to 20–60% sucrose gradients and equilibrium ultracentrifugation. Eleven fractions were harvested from the top of the sucrose gradients and used to determine the density, HCV RNA levels, infectivity titer, and HCV core amounts. ( a ) The buoyant density of sucrose was plotted with the HCV RNA level as measured by qRT-PCR in each fraction. ( b ) The HCV infectivity of each fraction was evaluated. ( c ) Left: Western blot analysis of the <t>ApoE</t> and core protein levels in each fraction of the sucrose gradient. The right panel displays the relative core-to-total-core amounts as detected in all fractions. ( d ) Western blot analysis of ApoE from the indicated fractions of the sucrose gradient those were rich in HCV infectious particles. ( e ) Western blot analysis of total supernatants ApoE (left) and cell lysates ApoE (right). ( f ) The effect <t>of</t> <t>CIDEB</t> silencing on the co-localization of NS5A-EGFP with endogenous ApoE in HCV- Jc1EGFP persistently infected Huh7.5.1 cells. The magnification of the frame section of merged images is presented at the right of the merged images. ( g ) The effect of CIDEB silencing on NS5A-ApoE and E2-ApoE co-localization was evaluated by overlap efficiency. ( h ) The effect of CIDEB silencing on the NS5A-ApoE interaction. Huh7.5.1 cells were transduced with Flag-NS5A and HA-ApoE lentivirus for 48 h and then treated with siNC or siCIDEB for 72 h. Cell lysates were subjected to IP with an anti-Flag antibody and then immunoblotted with an anti-HA antibody.
Anti Rabbit Apoe Antibody 381129, supplied by ZenBio, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+apoe+antibody/anti+rabbit+apoe+antibody+381129/pm40245754-56-0-16
Average 90 stars, based on 1 article reviews
anti-rabbit apoe antibody 381129 - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
rabbit polyclonal antibodies specific for human apoai, apoaii, apoe, saa, or aβ (1–42)  (Cosmo Bio USA)
90
Cosmo Bio USA rabbit polyclonal antibodies specific for human apoai, apoaii, apoe, saa, or aβ (1–42)
( a–c ) Concentrated culture supernatants from HCV persistently infected Huh7.5.1 cells treated with siRNAs were subjected to 20–60% sucrose gradients and equilibrium ultracentrifugation. Eleven fractions were harvested from the top of the sucrose gradients and used to determine the density, HCV RNA levels, infectivity titer, and HCV core amounts. ( a ) The buoyant density of sucrose was plotted with the HCV RNA level as measured by qRT-PCR in each fraction. ( b ) The HCV infectivity of each fraction was evaluated. ( c ) Left: Western blot analysis of the <t>ApoE</t> and core protein levels in each fraction of the sucrose gradient. The right panel displays the relative core-to-total-core amounts as detected in all fractions. ( d ) Western blot analysis of ApoE from the indicated fractions of the sucrose gradient those were rich in HCV infectious particles. ( e ) Western blot analysis of total supernatants ApoE (left) and cell lysates ApoE (right). ( f ) The effect <t>of</t> <t>CIDEB</t> silencing on the co-localization of NS5A-EGFP with endogenous ApoE in HCV- Jc1EGFP persistently infected Huh7.5.1 cells. The magnification of the frame section of merged images is presented at the right of the merged images. ( g ) The effect of CIDEB silencing on NS5A-ApoE and E2-ApoE co-localization was evaluated by overlap efficiency. ( h ) The effect of CIDEB silencing on the NS5A-ApoE interaction. Huh7.5.1 cells were transduced with Flag-NS5A and HA-ApoE lentivirus for 48 h and then treated with siNC or siCIDEB for 72 h. Cell lysates were subjected to IP with an anti-Flag antibody and then immunoblotted with an anti-HA antibody.
Rabbit Polyclonal Antibodies Specific For Human Apoai, Apoaii, Apoe, Saa, Or Aβ (1–42), supplied by Cosmo Bio USA, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rabbit+apoe+antibody/rabbit+polyclonal+antibodies+specific+for+human+apoai++apoaii++apoe++saa++or+a%CE%B2++1+42+/pm16651021-105-20-25
Average 90 stars, based on 1 article reviews
rabbit polyclonal antibodies specific for human apoai, apoaii, apoe, saa, or aβ (1–42) - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
apolipoprotein e apoe rabbit polyclonal antibody  (OriGene)
N/A
Apolipoprotein E APOE rabbit polyclonal antibody Serum
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apolipoprotein e apoe isoform e3 rabbit polyclonal antibody  (OriGene)
N/A
Apolipoprotein E APOE Isoform E3 rabbit polyclonal antibody Biotin
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rabbit anti-human apoe polyclonal antibody  (Cusabio)
N/A
Rabbit anti-Human APOE Polyclonal Antibody
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Image Search Results


( a–c ) Concentrated culture supernatants from HCV persistently infected Huh7.5.1 cells treated with siRNAs were subjected to 20–60% sucrose gradients and equilibrium ultracentrifugation. Eleven fractions were harvested from the top of the sucrose gradients and used to determine the density, HCV RNA levels, infectivity titer, and HCV core amounts. ( a ) The buoyant density of sucrose was plotted with the HCV RNA level as measured by qRT-PCR in each fraction. ( b ) The HCV infectivity of each fraction was evaluated. ( c ) Left: Western blot analysis of the ApoE and core protein levels in each fraction of the sucrose gradient. The right panel displays the relative core-to-total-core amounts as detected in all fractions. ( d ) Western blot analysis of ApoE from the indicated fractions of the sucrose gradient those were rich in HCV infectious particles. ( e ) Western blot analysis of total supernatants ApoE (left) and cell lysates ApoE (right). ( f ) The effect of CIDEB silencing on the co-localization of NS5A-EGFP with endogenous ApoE in HCV- Jc1EGFP persistently infected Huh7.5.1 cells. The magnification of the frame section of merged images is presented at the right of the merged images. ( g ) The effect of CIDEB silencing on NS5A-ApoE and E2-ApoE co-localization was evaluated by overlap efficiency. ( h ) The effect of CIDEB silencing on the NS5A-ApoE interaction. Huh7.5.1 cells were transduced with Flag-NS5A and HA-ApoE lentivirus for 48 h and then treated with siNC or siCIDEB for 72 h. Cell lysates were subjected to IP with an anti-Flag antibody and then immunoblotted with an anti-HA antibody.

Journal: Scientific Reports

Article Title: Cell-death-inducing DFFA-like Effector B Contributes to the Assembly of Hepatitis C Virus (HCV) Particles and Interacts with HCV NS5A

doi: 10.1038/srep27778

Figure Lengend Snippet: ( a–c ) Concentrated culture supernatants from HCV persistently infected Huh7.5.1 cells treated with siRNAs were subjected to 20–60% sucrose gradients and equilibrium ultracentrifugation. Eleven fractions were harvested from the top of the sucrose gradients and used to determine the density, HCV RNA levels, infectivity titer, and HCV core amounts. ( a ) The buoyant density of sucrose was plotted with the HCV RNA level as measured by qRT-PCR in each fraction. ( b ) The HCV infectivity of each fraction was evaluated. ( c ) Left: Western blot analysis of the ApoE and core protein levels in each fraction of the sucrose gradient. The right panel displays the relative core-to-total-core amounts as detected in all fractions. ( d ) Western blot analysis of ApoE from the indicated fractions of the sucrose gradient those were rich in HCV infectious particles. ( e ) Western blot analysis of total supernatants ApoE (left) and cell lysates ApoE (right). ( f ) The effect of CIDEB silencing on the co-localization of NS5A-EGFP with endogenous ApoE in HCV- Jc1EGFP persistently infected Huh7.5.1 cells. The magnification of the frame section of merged images is presented at the right of the merged images. ( g ) The effect of CIDEB silencing on NS5A-ApoE and E2-ApoE co-localization was evaluated by overlap efficiency. ( h ) The effect of CIDEB silencing on the NS5A-ApoE interaction. Huh7.5.1 cells were transduced with Flag-NS5A and HA-ApoE lentivirus for 48 h and then treated with siNC or siCIDEB for 72 h. Cell lysates were subjected to IP with an anti-Flag antibody and then immunoblotted with an anti-HA antibody.

Article Snippet: The following antibodies were used: anti-HCV core antibody (C7-50, Abcam), anti-HCV NS3 antibody (H23, Abcam), monoclonal mouse GFP antibody (AG281, Beyotime), monoclonal mouse anti-Flag antibody (F1804, Sigma), monoclonal mouse HA antibody (AH158, Beyotime), polyclonal rabbit HA Antibody (Sc-805, Santa Cruz), anti-DENV NS1 antibody (ab41616, Abcam), anti-β-actin antibody (BioVision), anti-CIDEB monoclonal antibody (M01, Abnova), anti-ApoE antibody (10817-RP02, Sino Biological), polyclonal anti-CIDEB antibody (LS-C119539, Lifespan), goat anti-mouse antibody (Chemicon), goat anti-rabbit antibody (Chemicon) conjugated with horseradish peroxidase, Cy3-labeled goat anti-mouse IgG (H + L) (Beyotime), Alexa Fluor 647-labeled goat anti-rabbit IgG (Beyotime), Alexa Fluor 555-labeled donkey anti-rabbit IgG (H + L) (Beyotime) and Alexa Fluor 488-labeled donkey anti-mouse IgG (H + L) (Invitrogen).

Techniques: Infection, Quantitative RT-PCR, Western Blot, Transduction

( a ) CIDEB participates in HCV assembly and interacts with NS5A. By localizing on the smooth ER and LDs by its C terminus, the N terminus of CIDEB may interact with NS5A to influence the NS5A-ApoE interaction, which further affect the association of HCV particles with ApoE. ( b ) A proposed model for the interaction between CIDEB and NS5A. The N terminus of CIDEB and domain I of NS5A are involved in the CIDEB-NS5A interaction.

Journal: Scientific Reports

Article Title: Cell-death-inducing DFFA-like Effector B Contributes to the Assembly of Hepatitis C Virus (HCV) Particles and Interacts with HCV NS5A

doi: 10.1038/srep27778

Figure Lengend Snippet: ( a ) CIDEB participates in HCV assembly and interacts with NS5A. By localizing on the smooth ER and LDs by its C terminus, the N terminus of CIDEB may interact with NS5A to influence the NS5A-ApoE interaction, which further affect the association of HCV particles with ApoE. ( b ) A proposed model for the interaction between CIDEB and NS5A. The N terminus of CIDEB and domain I of NS5A are involved in the CIDEB-NS5A interaction.

Article Snippet: The following antibodies were used: anti-HCV core antibody (C7-50, Abcam), anti-HCV NS3 antibody (H23, Abcam), monoclonal mouse GFP antibody (AG281, Beyotime), monoclonal mouse anti-Flag antibody (F1804, Sigma), monoclonal mouse HA antibody (AH158, Beyotime), polyclonal rabbit HA Antibody (Sc-805, Santa Cruz), anti-DENV NS1 antibody (ab41616, Abcam), anti-β-actin antibody (BioVision), anti-CIDEB monoclonal antibody (M01, Abnova), anti-ApoE antibody (10817-RP02, Sino Biological), polyclonal anti-CIDEB antibody (LS-C119539, Lifespan), goat anti-mouse antibody (Chemicon), goat anti-rabbit antibody (Chemicon) conjugated with horseradish peroxidase, Cy3-labeled goat anti-mouse IgG (H + L) (Beyotime), Alexa Fluor 647-labeled goat anti-rabbit IgG (Beyotime), Alexa Fluor 555-labeled donkey anti-rabbit IgG (H + L) (Beyotime) and Alexa Fluor 488-labeled donkey anti-mouse IgG (H + L) (Invitrogen).

Techniques: