Anti-RYBP 抗体 [EPR13059(2)] - BSA and Azide free
Anti-RYBP antibody [EPR13059(2)] - BSA and Azide free
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal RYBP antibody. Carrier free. Suitable for IP, ChIP, WB, IHC-P, ICC/IF, Flow Cyt (Intra) and reacts with Mouse, Human, Rat samples.
別名を表示する
DEDAF, YEAF1, RYBP, RING1 and YY1-binding protein, Apoptin-associating protein 1, Death effector domain-associated factor, YY1 and E4TF1-associated factor 1, APAP-1, DED-associated factor
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-RYBP antibody [EPR13059(2)] - BSA and Azide free (AB250871)
Intracellular Flow Cytometry analysis of A431 (Human epidermoid carcinoma epithelial cell) cells labeling RYBP with purified ab185971 at 1/20 dilution (11.7μg/mL) (Red). Cells were fixed with 4% paraformaldehyde and permeabilised with 90% methanol. A Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) secondary antibody was used at 1/2000 dilution. Isotype control - Rabbit monoclonal IgG (ab172730) (black). Unlabeled control - Unlabelled cells (blue). This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab185971).
- IP
Lab
Immunoprecipitation - Anti-RYBP antibody [EPR13059(2)] - BSA and Azide free (AB250871)
This data was developed using ab185971, the same antibody clone in a different buffer formulation.
RYBP was immunoprecipitated from HEK-293 (human embryonic kidney epithelial cell) whole cell lysate 10 μg with ab185971 1/1000 dilution. Western blot was performed on the immunoprecipitate using ab185971 at 1/1000 dilution. Capture antibody, 1 : 30 dilution (2μg in 0.35mg lysates).
Rabbit monoclonal IgG (ab172730) Isotype Control was used instead of ab185971 in HEK-293 whole cell lysate (Lane 3).
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
To minimize protein degradation, cells were lysed immediately after harvest and then applied for Immunoprecipitation as soon as possible.
All lanes:
Immunoprecipitation - Anti-RYBP antibody [EPR13059(2)] - ChIP Grade (<a href='/products/primary-antibodies/rybp-antibody-epr130592-chip-grade-ab185971'>ab185971</a>) at 1/1000 dilution
Lane 1:
HEK-293 (human embryonic kidney epithelial cell) whole cell lysate (Low Expression Sample) 10 μg
Lane 2:
HEK-293 (human embryonic kidney epithelial cell) whole cell lysate
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
Observed band size: 32 kDa
false
Exposure time: 15s
- ChIP
Unknown
ChIP - Anti-RYBP antibody [EPR13059(2)] - BSA and Azide free (AB250871)
Chromatin was prepared from HEK293 cells according to the Abcam Dual X-ChIP protocol*. Cells were fixed with EGS for 30 minutes, then formaldehyde for 10 minutes.
The ChIP was performed with 25 μg of chromatin, 5 μg of ab185971 (red), and 20 μl of Protein A/G sepharose beads. 5 μg of rabbit normal IgG was added to the beads control (gray). The immunoprecipitated DNA was quantified by real time PCR (Sybr green approach).
Primers and probes are located in the first kb of the transcribed region.
*http : //www.abcam.com/resources?keywords=X%20ChIP%20protocol
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab185971).
- IP
Lab
Immunoprecipitation - Anti-RYBP antibody [EPR13059(2)] - BSA and Azide free (AB250871)
This data was developed using ab185971, the same antibody clone in a different buffer formulation.
RYBP was immunoprecipitated from NIH/3T3 (mouse embryonic fibroblast) whole cell lysate 10 μg with ab185971 1/1000 dilution. Western blot was performed on the immunoprecipitate using ab185971 at 1/1000 dilution. Capture antibody, 1 : 30 dilution (2μg in 0.35mg lysates).
Rabbit monoclonal IgG (ab172730) Isotype Control was used instead of ab185971 in NIH/3T3 whole cell lysate (Lane 3).
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
To minimize protein degradation, cells were lysed immediately after harvest and then applied for Immunoprecipitation as soon as possible.
All lanes:
Immunoprecipitation - Anti-RYBP antibody [EPR13059(2)] - ChIP Grade (<a href='/products/primary-antibodies/rybp-antibody-epr130592-chip-grade-ab185971'>ab185971</a>) at 1/1000 dilution
Lane 1:
NIH/3T3 (mouse embryonic fibroblast) whole cell lysate (Low Expression Sample) 10 μg
Lane 2:
NIH/3T3 (mouse embryonic fibroblast) whole cell lysate
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
Observed band size: 32 kDa
false
Exposure time: 24s
- ChIP
Unknown
ChIP - Anti-RYBP antibody [EPR13059(2)] - BSA and Azide free (AB250871)
Chromatin was prepared from NIH/3T3 cells according to the Abcam Dual X-ChIP protocol*. Cells were fixed with EGS for 30 minutes, then formaldehyde for 10 minutes.
The ChIP was performed with 25 μg of chromatin, 5 μg of ab185971 (red), and 20 μl of Protein A/G sepharose beads. 5 μg of rabbit normal IgG was added to the beads control (gray). The immunoprecipitated DNA was quantified by real time PCR (Sybr green approach).
Primers and probes are located in the first kb of the transcribed region.
*http : //www.abcam.com/resources?keywords=X%20ChIP%20protocol
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab185971).
関連する標識済み抗体及び組成の異なる製品 (10)
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Anti-RYBP antibody [EPR13059(2)] - ChIP Grade
-
775 Alexa Fluor® 750
Alexa Fluor® 750 Anti-RYBP antibody [EPR13059(2)] - ChIP Grade
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578 PE
PE Anti-RYBP antibody [EPR13059(2)]
-
660 APC
APC Anti-RYBP antibody [EPR13059(2)]
-
HRP Anti-RYBP antibody [EPR13059(2)]
-
519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-RYBP antibody [EPR13059(2)]
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665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-RYBP antibody [EPR13059(2)]
-
617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-RYBP antibody [EPR13059(2)]
-
565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-RYBP antibody [EPR13059(2)]
-
603 Alexa Fluor® 568
Alexa Fluor® 568 Anti-RYBP antibody [EPR13059(2)]
Reactivity data
製品の詳細
ab250871 is the carrier-free version of ab185971.
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.
出荷温度及び保存条件
製品の状態
精製方法
バッファー組成
出荷温度
短期保存温度
長期保存温度
保管に関する情報
補足情報
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
This protein actively participates in maintaining transcriptional repression through its involvement in the Polycomb Repressive Complex 1 (PRC1). PRC1 includes other key proteins such as Ring1A/B and CBX proteins which work together to modulate chromatin structure. RYBP contributes to the ubiquitination of histone H2A a process essential for maintaining gene silencing. This activity is important during developmental stages influencing cell fate decisions and lineage commitment.
Pathways
RYBP plays an essential role in the regulation of the Wnt signaling pathway and the apoptosis pathway. Within the Wnt pathway RYBP acts in part by interacting with proteins such as β-catenin influencing cell proliferation and differentiation. In the apoptosis pathway it is involved through its interactions with E3 ubiquitin ligases potentially affecting cell death regulation. These pathways showcase how RYBP integrates into important cellular processes impacting cellular homeostasis.
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ターゲットの情報
Abcam product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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