Anti-Hsp90 antibody [AC88]
4
(30 리뷰들)
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(158 제품이 사용된 논문 )
- Over 130 publications
- Trusted since 2004
- WB
Unknown
Western blot - Anti-Hsp90 antibody [AC88] (AB13492)
This image was generated using the ascites version of the product.
All lanes:
Western blot - Anti-Hsp90 antibody [AC88] (ab13492) at 1/1000 dilution
Lane 1:
Hsp90 native human protein
Lane 2:
Hsp90 beta reombinant human protein
Lane 3:
Hsp90 alpha reombinant human protein
Lane 4:
Cell lysates prepared from heat shocked Hela cells
Lane 5:
Cell lysates prepared from heat shocked 3T3 cells
Lane 6:
Cell lysates prepared from heat shocked PC-12 cells
Lane 7:
Cell lysates prepared from heat shocked CHO-K1 cells
Lane 8:
Cell lysates prepared from heat shocked Rat-2 cells
Predicted band size: 85 kDa
false
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Hsp90 antibody [AC88] (AB13492)
ab13492 staining Hsp90 in Human spleen tissue sections by Immunohistochemistry (IHC-P - paraformaldehyde-fixed, paraffin-embedded sections). Samples were incubated with primary antibody (10 ug/ml).
This image was generated using the ascites version of the product.
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-Hsp90 antibody [AC88] (AB13492)
Overlay histogram showing HeLa cells stained with ab13492 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum (ab7481) / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab13492, 1μg/1x106 cells) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was mouse IgG1 [ICIGG1] (ab91353, 2μg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed.
This image was generated using the ascites version of the product.
- IHC-P
AbReview42064****
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Hsp90 antibody [AC88] (AB13492)
ab13492 staining Hsp90 in Human testis tissue sections by Immunohistochemistry (IHC-P - paraformaldehyde-fixed, paraffin-embedded sections). Tissue was fixed with paraformaldehyde and antigen retrieval was by heat mediation in a TRIS-EDTA Buffer. Samples were incubated with primary antibody (1/500) for 30 minutes at 20°C. A HRP-conjugated Goat anti-rabbit/mouse IgG polyclonal was used as the secondary antibody.
This image was generated using the ascites version of the product.
This image is courtesy of an Abreview submitted by Rudolf Jung
- ICC/IF
AbReview39468****
Immunocytochemistry/ Immunofluorescence - Anti-Hsp90 antibody [AC88] (AB13492)
ab13492 staining Hsp90 (red) and another antibody to C2GnT-M (Golgi enzyme, greeen) in Panc-1 cells by ICC/IF (Immunocytochemistry/immunofluorescence). Cells were fixed with PFA and blocked with 1% serum for 1 hour at 22°C. Samples were incubated with primary antibody (1/50 1% Donkey serum in PBST) for 1 hour at 22°C. An undiluted DyLight® 594-conjugated Donkey anti-mouse IgG polyclonal was used as the secondary antibody.
This image was generated using the ascites version of the product.
This image is courtesy of an Abreview submitted by Armen Petrosyan
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-Hsp90 antibody [AC88] (AB13492)
ICC/IF image of ab13492 stained HepG2 cells (ab7900). The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab13492, 5μg/ml) overnight at +4°C. The secondary antibody (green) was DyLight® 488 goat anti-mouse IgG - H&L, pre-adsorbed (ab96879) used at a 1/250 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43μM.
This image was generated using the ascites version of the product.
- WB
AbReview30510****
Western blot - Anti-Hsp90 antibody [AC88] (AB13492)
Blocked with 5% Milk for 2 hours at 22°C
This image was generated using the ascites version of the product.
All lanes:
Western blot - Anti-Hsp90 antibody [AC88] (ab13492) at 1/1000 dilution
All lanes:
Human fibroblast whole cell lysate at 40 µg
Secondary
All lanes:
HRP-conjugated goat anti-mouse polyclonal IgG at 1/2000 dilution
Predicted band size: 85 kDa
true
Exposure time: 20s
This image is courtesy of an anonymous Abreview
- WB
Supplier Data
Western blot - Anti-Hsp90 antibody [AC88] (AB13492)
This image was generated using the ascites version of the product.
All lanes:
Western blot - Anti-Hsp90 antibody [AC88] (ab13492) at 1/1000 dilution
Lane 2:
HSP90 cell lysate
Lane 3:
HSP90β cell lysate
Lane 4:
HSP90α cell lysate
Lane 5:
HeLa (heat shocked) cell lysate
Lane 6:
NIH/3T3 (Heat shocked) cell lysate
Lanes 7 - 8:
PC-12 (Heat shocked) cell lysate
Predicted band size: 85 kDa
false
Reactivity 정보
제품 세부 정보
Anti-Hsp90 antibody [AC88] (ab13492) is a mouse monoclonal antibody and is validated for use in Western Blot (WB), Flow Cytometry (Intra), Flow Cytometry (Flow Cyt), Immunohistochemistry (IHC-P), Immunocytochemistry/immunofluorescence (ICC/IF) in Chinese hamster, Human, Mouse, Rat samples.
Trusted by the scientific community
Anti-Hsp90 [AC88] (ab13492) was first used in a scientific publication in 2004 and has been cited over 130 times in peer-reviewed journals.
Reviewed by scientists
Anti-Hsp90 [AC88] (ab13492) has over 30 independent reviews from customers.
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
Hsp90 interacts with many co-chaperones to form multi-protein complexes that aid its function. This protein is necessary for the maturation and stability of many signaling proteins including steroid hormone receptors and kinases like the tyrosine kinase D7A. Hsp90's chaperone activity is ATP-dependent with its N-terminal domain binding and hydrolyzing ATP leading to conformational changes that promote protein folding and assembly. Its influence extends to regulating cell cycle control and apoptosis highlighting its importance in cellular processes.
Pathways
Hsp90 participates in key biological pathways such as the protein folding response and the MAPK signaling pathway. In the protein folding process Hsp90 collaborates with co-chaperones like Aha1 and p23 to ensure accurate protein synthesis and repair. Its role in the MAPK signaling pathway influences cell growth proliferation and differentiation interacting with proteins like Raf-1 and MEK. These interactions highlight Hsp90's involvement in signal transduction and cellular stress responses.
제품 프로토콜
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제품이 사용된 논문 (158)
Recent publications for all applications. Explore the 전체 목록 and refine your search
Discover oncology 16:1540 PubMed40796704
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Scientific reports 15:10532 PubMed40148452
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World journal of gastroenterology 31:103412 PubMed40124262
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Journal of translational medicine 23:172 PubMed39930487
2025
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International journal of molecular sciences 25: PubMed39409021
2024
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Foods (Basel, Switzerland) 13: PubMed39335893
2024
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Nucleic acids research 52:12351-12377 PubMed39315696
2024
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Nutrients 16: PubMed39125387
2024
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Nature communications 15:6626 PubMed39103353
2024
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International journal of molecular sciences 25: PubMed38892076
2024
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Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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