Anti-ADK antibody [EPR27497-67] - BSA and Azide free
- RabMAb
- Recombinant
- KO Validated
- 각 태그의 뜻
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- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-ADK antibody [EPR27497-67] - BSA and Azide free (AB307358)
This data was developed using ab307357, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized ADK KO HAP1 (ADK knockout human chronic myelogenous leukemia near-haploid cell) cells labeling ADK with ab307357 at 1/50 dilution (10.64 µg/ml), followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution (2 µg/ml) (Green). Confocal image showing nuclear and weak cytoplasmic staining in wildtype HAP1 cells, and no staining in ADK knockout HAP1 cells. The image was taken with a confocal microscope (Leica-Microsystems, TCS SP8). ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (2.5 µg/ml) (Red). Nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution (2 µg/ml).
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-ADK antibody [EPR27497-67] - BSA and Azide free (AB307358)
This data was developed using ab307357, the same antibody clone in a different buffer formulation. Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized wild-type HAP1 (human chronic myelogenous leukemia near-haploid cell) (Right) / ADK knockout HAP1 (Left) cells labeling ADK with ab307357 at 1/50 dilution (1µg) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat anti-Rabbit IgG (Alexa Fluor® 647, ab150083) at 1/2000 dilution was used as the secondary antibody.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-ADK antibody [EPR27497-67] - BSA and Azide free (AB307358)
This data was developed using ab307357, the same antibody clone in a different buffer formulation. Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized NIH/3T3 (mouse embryonic fibroblast) cells labeling ADK with ab307357 at 1/50 dilution (1µg) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat anti-Rabbit IgG (Alexa Fluor® 647, ab150083) at 1/2000 dilution was used as the secondary antibody.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-ADK antibody [EPR27497-67] - BSA and Azide free (AB307358)
This data was developed using ab307357, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized NIH/3T3 (mouse embryonic fibroblast) cells labeling ADK with ab307357 at 1/50 dilution (10.64 µg/ml), followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution (2 µg/ml) (Green). Confocal image showing nuclear and weak cytoplasmic staining in NIH/3T3 cells. The image was taken with a confocal microscope (Leica-Microsystems, TCS SP8). ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (2.5 µg/ml) (Red). Nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution (2 µg/ml).
- IP
Supplier Data
Immunoprecipitation - Anti-ADK antibody [EPR27497-67] - BSA and Azide free (AB307358)
This data was developed using ab307357, the same antibody clone in a different buffer formulation. ADK was immunoprecipitated from 0.35 mg RAW264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate 10 µg with ab307357 at 1/30 dilution (2µg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab307357 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution. Lane 1 : RAW264.7 whole cell lysate 10 µg Lane 2 : ab307357 IP in RAW264.7 whole cell lysate Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab307357 in RAW264.7 whole cell lysate Blocking and dilution buffer and concentration : 5% NFDM/TBST. Exposure time : 128 seconds
All lanes:
Immunoprecipitation - Anti-ADK antibody [EPR27497-67] (<a href='/ko/products/primary-antibodies/adk-antibody-epr27497-67-ab307357'>ab307357</a>) at 1/1000 dilution
Lane 1:
RAW264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate
Lane 2:
RAW264.7 whole cell lysate
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/ko/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
Observed band size: 45 kDa
false
Exposure time: 128s
- IP
Supplier Data
Immunoprecipitation - Anti-ADK antibody [EPR27497-67] - BSA and Azide free (AB307358)
This data was developed using ab307357, the same antibody clone in a different buffer formulation. ADK was immunoprecipitated from 0.35 mg C6 (rat glial tumor glial cell) whole cell lysate 10 µg with ab307357 at 1/30 dilution (2µg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab307357 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution. Lane 1 : C6 whole cell lysate 10 µg Lane 2 : ab307357 IP in C6 whole cell lysate Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab307357 in C6 whole cell lysate Blocking and dilution buffer and concentration : 5% NFDM/TBST. Exposure time : 128 seconds.
All lanes:
Immunoprecipitation - Anti-ADK antibody [EPR27497-67] (<a href='/ko/products/primary-antibodies/adk-antibody-epr27497-67-ab307357'>ab307357</a>) at 1/1000 dilution
Lane 1:
C6 (rat glial tumor glial cell) whole cell lysate
Lane 2:
C6 whole cell lysate
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/ko/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
Observed band size: 45 kDa
false
Exposure time: 128s
- WB
Supplier Data
Western blot - Anti-ADK antibody [EPR27497-67] - BSA and Azide free (AB307358)
This data was developed using 307357, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : Low expression : A549 In Western blot, ab307357 was shown to bind specifically to ADK. A band was observed at 45 kDa in wild-type HAP1 cell lysates whereas no signal observed at this size in ADK knockout cell line. This blot (lanes 1-4) was developed using a high sensitivity ECL substrate. 125 seconds Exposure time :
All lanes:
Western blot - Anti-ADK antibody [EPR27497-67] (<a href='/ko/products/primary-antibodies/adk-antibody-epr27497-67-ab307357'>ab307357</a>) at 1/1000 dilution
Lane 1:
Wild-type HAP1 whole cell lysate
Lane 2:
ADK knockout HAP1 whole cell lysate
Lane 3:
HeLa whole cell lysate
Lane 4:
A549 whole cell lysate
Lane 5:
RAW264.7 whole cell lysate
Lane 6:
C6 whole cell lysate
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
Observed band size: 45 kDa
true
Exposure time: 125s
- WB
Supplier Data
Western blot - Anti-ADK antibody [EPR27497-67] - BSA and Azide free (AB307358)
This data was developed using 307357, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST Low expression : mouse heart (PMID : 15930047;14736855), rat heart (PMID : 15930047;14736855). Exposure time : 15 seconds
All lanes:
Western blot - Anti-ADK antibody [EPR27497-67] (<a href='/ko/products/primary-antibodies/adk-antibody-epr27497-67-ab307357'>ab307357</a>) at 1/1000 dilution
Lane 1:
Mouse liver tissue lysate
Lane 2:
Rat liver tissue lysate
Lane 3:
Mouse heart tissue lysate
Lane 4:
Rat heart tissue lysate
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
Observed band size: 45 kDa
false
Exposure time: 15s
관련 conjugated 항체와 다양한 조성의 항체 (1)
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Anti-ADK antibody [EPR27497-67]
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.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
특성 및 보관 정보
제형
Purification 테크닉
보관 버퍼
배송 시 보관 조건
적절한 단기 보관 조건
적절한 장기 보관 조건
추가 정보
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The enzyme modulates cellular adenosine levels which influences various physiological functions such as sleep regulation and immune responses. ADK does not operate as part of a larger protein complex but acts independently to maintain intracellular energy balance by regulating the pools of adenosine and AMP. The enzyme activity affects purine metabolism important in diverse cellular activities.
Pathways
The activity of adenosine kinase fits prominently into the purine metabolism and energy homeostasis pathways. Its function maintains the cellular concentrations of adenosine a nucleotide affecting cellular signaling pathways including the AMP-activated protein kinase (AMPK) pathway. ADK interacts with enzymes like adenosine deaminase which collectively orchestrate the purine salvage pathway—pivotal in nucleotide recycling.
제품 프로토콜
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타겟 정보
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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