Anti-CITED2 antibody [EPR27399-62] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
- 각 태그의 뜻
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Rabbit Recombinant Monoclonal CITED2 antibody. Carrier free. Suitable for IHC-P, WB, IP, ICC/IF, Dot and reacts with Mouse, Rat, Human, Recombinant full length protein - Human samples.
대체 명칭 보기
MRG1, CITED2, Cbp/p300-interacting transactivator 2, MSG-related protein 1, P35srj, MRG-1
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-CITED2 antibody [EPR27399-62] - BSA and Azide free (AB314758)
This data was developed using ab314757, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized HT-1080 (human fibrosarcoma epithelial cell) cells labelling CITED2 with ab314757 at 1/50 (10.34 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2ug/ml) dilution (Green). Confocal image showing nuclear staining in HT-1080 cell line. 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 (2.5ug/ml) dilution (Red). The 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 (2ug/ml) dilution.
- IP
Supplier Data
Immunoprecipitation - Anti-CITED2 antibody [EPR27399-62] - BSA and Azide free (AB314758)
This data was developed using ab314757, the same antibody clone in a different buffer formulation. CITED2 was immunoprecipitated from 0.35 mg K-562 (human chronic myelogenous leukemia lymphoblast) whole cell lysate with ab314757 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab314757 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution. Lane 1 : K-562 (human chronic myelogenous leukemia lymphoblast) whole cell lysate 10 ug Lane 2 : ab314757 IP in K-562 (human chronic myelogenous leukemia lymphoblast) whole cell lysate Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab314757 in K-562 whole cell lysate Blocking and dilution buffer and concentration : 5% NFDM/TBST.
All lanes:
Immunoprecipitation - Anti-CITED2 antibody [EPR27399-62] (<a href='/ko/products/primary-antibodies/cited2-antibody-epr27399-62-ab314757'>ab314757</a>) at 1/30 dilution
All lanes:
K-562 (human chronic myelogenous leukemia lymphoblast) 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
false
Exposure time: 3min
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CITED2 antibody [EPR27399-62] - BSA and Azide free (AB314758)
This data was developed using ab314757, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded mouse cerebrum tissue labeling CITED2 with ab314757 at 1/500 (1.034 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Nuclear staining on mouse cerebrum. The section was incubated with ab314757 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CITED2 antibody [EPR27399-62] - BSA and Azide free (AB314758)
This data was developed using ab314757, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded mouse pancreatic cancer tissue labeling CITED2 with ab314757 at 1/500 (1.034 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Nuclear staining on mouse pancreatic cancer. The section was incubated with ab314757 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CITED2 antibody [EPR27399-62] - BSA and Azide free (AB314758)
This data was developed using ab314757, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded mouse colon tissue labeling CITED2 with ab314757 at 1/500 (1.034 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Nuclear staining on mouse colon. The section was incubated with ab314757 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CITED2 antibody [EPR27399-62] - BSA and Azide free (AB314758)
This data was developed using ab314757, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded rat colon tissue labeling CITED2 with ab314757 at 1/500 (1.034 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Nuclear staining on rat colon. The section was incubated with ab314757 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CITED2 antibody [EPR27399-62] - BSA and Azide free (AB314758)
This data was developed using ab314757, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded rat cerebrum tissue labeling CITED2 with ab314757 at 1/500 (1.034 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Nuclear staining on rat cerebrum. The section was incubated with ab314757 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IP
Supplier Data
Immunoprecipitation - Anti-CITED2 antibody [EPR27399-62] - BSA and Azide free (AB314758)
This data was developed using ab314757, the same antibody clone in a different buffer formulation. CITED2 was immunoprecipitated from 0.35 mg MEF (mouse embryo fibroblast) treated with 5 μM MG-132 for 6 hours whole cell lysate with ab314757 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab314757 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution. Lane 1 : MEF (mouse embryo fibroblast) treated with 5 μM MG-132 for 6 hours whole cell lysate Lane 2 : ab314757 IP in MEF (mouse embryo fibroblast) treated with 5 μM MG-132 for 6 hours whole cell lysate Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab314757 in MEF treated with 5 μM MG-132 for 6 hours whole cell lysate Blocking and dilution buffer and concentration : 5% NFDM/TBST.
All lanes:
Immunoprecipitation - Anti-CITED2 antibody [EPR27399-62] (<a href='/ko/products/primary-antibodies/cited2-antibody-epr27399-62-ab314757'>ab314757</a>) at 1/30 dilution
All lanes:
MEF (mouse embryo fibroblast) treated with 5 μM MG-132 for 6 hours 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
false
Exposure time: 3min
- WB
Lab
Western blot - Anti-CITED2 antibody [EPR27399-62] - BSA and Azide free (AB314758)
In Western blot, anti-GAPDH antibody (ab181602) loading control staining at 1/1000000 dilution.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
All lanes:
Western blot - Anti-CITED2 antibody [EPR27399-62] (<a href='/ko/products/primary-antibodies/cited2-antibody-epr27399-62-ab314757'>ab314757</a>) at 1/1000 dilution
Lane 1:
HeLa (human cervix adenocarcinoma epithelial cell) + si-Scramble whole cell lysate at 20 µg
Lane 2:
HeLa + si-CITED2 whole cell 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 1/20000 dilution
Observed band size: 30 kDa,36 kDa
false
Exposure time: 10s
- WB
Supplier Data
Western blot - Anti-CITED2 antibody [EPR27399-62] - BSA and Azide free (AB314758)
This data was developed using ab314757, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST Exposure time : Lane 1-3 : 48 seconds Lane 4 : 37 seconds
All lanes:
Western blot - Anti-CITED2 antibody [EPR27399-62] (<a href='/ko/products/primary-antibodies/cited2-antibody-epr27399-62-ab314757'>ab314757</a>) at 1/1000 dilution
Lane 1:
HeLa (human epithelial cell line from cervical adenocarcinoma) whole cell lysate at 20 µg
Lane 2:
293T (human embryonic kidney epithelial cell) whole cell lysate at 20 µg
Lane 3:
NIH/3T3 (mouse embryonic fibroblast) whole cell lysate at 20 µg
Lane 4:
K-562 (human chronic myelogenous leukemia lymphoblast) whole cell 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
Observed band size: 30 kDa
false
- WB
Supplier Data
Western blot - Anti-CITED2 antibody [EPR27399-62] - BSA and Azide free (AB314758)
This data was developed using ab314757, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The expression profile observed is consistent with what has been described in the literature (PMID : 17906695).
Lysates were freshly made and used immediately to minimize protein degradation.
In Western Blot, Anti HIF-1 alpha antibody [EPR16897-101] (ab179483) is applied at 1/1000 dilution to prove the DFO induction is successful.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-CITED2 antibody [EPR27399-62] (<a href='/ko/products/primary-antibodies/cited2-antibody-epr27399-62-ab314757'>ab314757</a>) at 1/1000 dilution
Lane 1:
Untreated HT-1080 (human fibrosarcoma epithelial cell) whole cell lysate at 20 µg
Lane 2:
HT-1080 treated with 0.5 mM DFO for 24 hours whole cell lysate at 20 µg
Lane 3:
HT-1080 treated with 0.5 mM DFO for 24 hours, then added 10uM MG-132 for 4 hours, whole cell lysate at 20 µg
Lane 4:
HT-1080 treated with 10uM MG-132 for 4 hours, whole cell 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
Observed band size: 30 kDa,36 kDa
false
Exposure time: 37s
- WB
Supplier Data
Western blot - Anti-CITED2 antibody [EPR27399-62] - BSA and Azide free (AB314758)
This data was developed using ab314757, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST Lysates were freshly made and used immediately to minimize protein degradation
All lanes:
Western blot - Anti-CITED2 antibody [EPR27399-62] (<a href='/ko/products/primary-antibodies/cited2-antibody-epr27399-62-ab314757'>ab314757</a>) at 1/1000 dilution
Lane 1:
Mouse brain tissue lysate at 20 µg
Lane 2:
Rat brain tissue 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
Observed band size: 30 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-CITED2 antibody [EPR27399-62] - BSA and Azide free (AB314758)
This data was developed using ab314757, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST The expression profile observed is consistent with what has been described in the literature (PMID : 17906695). The band beneath the target band (30 kDa) is expected to be degradation products. In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution. Exposure time : Lane 1, 2 : 15 seconds Lane 3, 4 : 103 seconds
All lanes:
Western blot - Anti-CITED2 antibody [EPR27399-62] (<a href='/ko/products/primary-antibodies/cited2-antibody-epr27399-62-ab314757'>ab314757</a>) at 1/1000 dilution
Lane 1:
Untreated MEF (mouse embryo fibroblast) whole cell lysate at 20 µg
Lane 2:
MEF treated with 5 uM MG-132 for 6 hours, whole cell lysate at 20 µg
Lane 3:
Untreated PC-12 (rat adrenal gland pheochromocytoma ) whole cell lysate at 20 µg
Lane 4:
PC-12 treated with 20 uM MG-132 for 5 hours, whole cell 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
Observed band size: 30 kDa,36 kDa
false
- Dot
Supplier Data
Dot Blot - Anti-CITED2 antibody [EPR27399-62] - BSA and Azide free (AB314758)
This data was developed using ab314757, the same antibody clone in a different buffer formulation. Dot blot analysis of CITED2 using ab314757 at 1 : 1000 (0.517 ug/ml) followed by a Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1 : 100,000 dilution. Exposure time : 48 seconds Blocking and diluting buffer and concentration : 5% NFDM/TBST
관련 conjugated 항체와 다양한 조성의 항체 (1)
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Anti-CITED2 antibody [EPR27399-62]
Reactivity 정보
제품 세부 정보
ab314758 is the carrier-free version of ab314757.
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
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적절한 장기 보관 조건
제품 프로토콜
- Visit the General protocols
- Visit the Troubleshooting
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