Anti-Apo-H antibody [EPR23087-228]
- BOND RX™ Validated
- RabMAb
- Recombinant
- 각 태그의 뜻
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Rabbit Recombinant Monoclonal Apo-H antibody. Suitable for IP, WB, ICC/IF, Flow Cyt (Intra), IHC-P and reacts with Human samples.
대체 명칭 보기
B2G1, APOH, Beta-2-glycoprotein 1, APC inhibitor, Activated protein C-binding protein, Anticardiolipin cofactor, Apolipoprotein H, Beta-2-glycoprotein I, Apo-H, B2GPI, Beta(2)GPI
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Apo-H antibody [EPR23087-228] (AB267464)
Immunohistochemical analysis of paraffin-embedded Human hepatocellular carcinoma tissue labeling Apo-H with ab267464 at 1/500 dilution (0.94 ug/ml) followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Positive staining on plasma in human hepatocellular carcinoma. The section was incubated with ab267464 for 15 mins at RT. The immunostaining staining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-Apo-H antibody [EPR23087-228] (AB267464)
Intracellular flow cytometric analysis of 4% paraformaldehyde fixed, 90% methanol permeabilized HeLa (human cervix adenocarcinoma epithelial cell, Left) / HepG2 (human hepatocellular carcinoma epithelial cell, Right) cells labelling Apo-H with ab267464 at 1/500 dilution (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) at 1/2000 dilution was used as the secondary antibody.
Negative control : HeLa (PMID : 14984368).
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-Apo-H antibody [EPR23087-228] (AB267464)
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized HepG2 (human hepatocellular carcinoma epithelial cell) cells labelling Apo-H with ab267464 at 1/100 dilution, followed by ab150077 AlexaFluor®488 Goat anti-Rabbit secondary antibody at 1/1000 dilution (Green). Confocal image showing cytoplasmic staining in HepG2 cell line, and no staining in Hela cells. Negative control : Hela (PMID : 14984368). ab195889 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (Red). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150077 AlexaFluor®488 Goat anti-Rabbit secondary at 1/1000 dilution.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Apo-H antibody [EPR23087-228] (AB267464)
Immunohistochemical analysis of paraffin-embedded Human colon tissue labeling Apo-H with ab267464 at 1/500 dilution (0.94 ug/ml) followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101). Positive staining on plasma in human colon. The section was incubated with ab267464 for 15 mins at RT. The immunostaining staining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins.
- IP
Unknown
Immunoprecipitation - Anti-Apo-H antibody [EPR23087-228] (AB267464)
Apo-H was immunoprecipitated from 0.35 mg HepG2 (human hepatocellular carcinoma epithelial cell) whole cell lysate with ab267464 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab267464 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366) was used at 1/1000 dilution.
Lane 1 : HepG2 (human hepatocellular carcinoma epithelial cell) whole cell lysate 10ug
Lane 2 : ab267464 IP in HepG2 whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab267464 in HepG2 whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 30 seconds
All lanes:
Immunoprecipitation - Anti-Apo-H antibody [EPR23087-228] (ab267464)
Predicted band size: 38 kDa
Observed band size: 50 kDa,60 kDa
false
- WB
Lab
Western blot - Anti-Apo-H antibody [EPR23087-228] (AB267464)
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/1000000 dilution.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
In Western blot analysis, ab108348 exhibited lower sensitivity compared to ab267464, for which reason we recommend ab108348 as superior alternative.
Protocol optimizations including increased protein loading (30-50 μg/lane), reduced primary antibody dilution (1 : 500), and fg-grade ECL substrates are suggested if ab267464 must be used.
Lane 1:
Western blot - Anti-Apo-H antibody [EPR2898(2)] (<a href='/ko/products/primary-antibodies/apo-h-antibody-epr28982-ab108348'>ab108348</a>) at 1/1000 dilution
Lane 2:
Western blot - Anti-Apo-H antibody [EPR23087-228] (ab267464) at 1/1000 dilution
All lanes:
HepG2 (human hepatocellular carcinoma epithelial cell) whole cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 50 kDa,60 kDa
false
Exposure time: 60s
- WB
Unknown
Western blot - Anti-Apo-H antibody [EPR23087-228] (AB267464)
Blocking and dilution buffer : 5% NFDM/TBST.
Exposure time : 147 seconds.
The molecular weight observed is consistent with what has been described in the literature (PMID : 30894461)
Negative control : Hela (PMID : 14984368).
All lanes:
Western blot - Anti-Apo-H antibody [EPR23087-228] (ab267464) at 1/1000 dilution
Lane 1:
HepG2 (human hepatocellular carcinoma epithelial cell) whole cell lysate at 20 µg
Lane 2:
HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 3:
Human liver lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/ko/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 38 kDa
Observed band size: 50 kDa,60 kDa
false
- WB
Unknown
Western blot - Anti-Apo-H antibody [EPR23087-228] (AB267464)
Blocking and dilution buffer : 5% NFDM/TBST.
Exposure time : 180 seconds.
The molecular weight observed is consistent with what has been described in the literature (PMID : 30894461).
All lanes:
Western blot - Anti-Apo-H antibody [EPR23087-228] (ab267464) at 1/1000 dilution
All lanes:
Human plasma at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/ko/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 38 kDa
Observed band size: 50 kDa
false
관련 conjugated 항체와 다양한 조성의 항체 (1)
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Anti-Apo-H antibody [EPR23087-228] - BSA and Azide free
Reactivity 정보
제품 세부 정보
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
특성 및 보관 정보
제형
Purification 테크닉
보관 버퍼
배송 시 보관 조건
적절한 단기 보관 기간
적절한 단기 보관 조건
적절한 장기 보관 조건
분주 정보
보관 정보
추가 정보
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Apo-H acts as an anticoagulant and participates in the modulation of immune response. It forms complexes with lipid-bound proteins facilitating the clearance of these complexes from the bloodstream. This interaction is key in processes like platelet aggregation and stabilization of membranes. Apo-H also influences the removal of oxidized proteins and lipids reducing cellular stress and preventing tissue damage.
Pathways
Apo-H plays a critical role in the coagulation cascade and lipid metabolism. It interacts with proteins such as prothrombin and fibrinogen influencing blood coagulation pathways. Apo-H's involvement in the clearance of apoptotic cells integrates into the lipid metabolic pathway highlighting its relationship with apolipoproteins and other lipid-related proteins. These interactions illustrate the multi-functional aspects of Apo-H within these pathways.
제품 프로토콜
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타겟 정보
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com