Anti-CSDE1/NRU antibody [EPR17413] - BSA and Azide free
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal CSDE1/NRU antibody. Carrier free. Suitable for IP, WB and reacts with Human, Mouse, Rat samples.
View Alternative Names
D1S155E, KIAA0885, NRU, UNR, CSDE1, Cold shock domain-containing protein E1, N-ras upstream gene protein, Protein UNR
- IP
Supplier Data
Immunoprecipitation - Anti-CSDE1/NRU antibody [EPR17413] - BSA and Azide free (AB251319)
This data was developed using ab200663, the same antibody clone in a different buffer formulation.
CSDE1/NRU was immunoprecipitated from 1mg of HeLa (Human epithelial cells from cervix adenocarcinoma) whole cell lysate with ab200663 at 1/140 dilution. Western blot was performed from the immunoprecipitate using ab200663 at 1/1000 dilution (Panel A) or ab201688 at 1/1000 dilution (Panel B). VeriBlot for IP Detection Reagent (HRP) (ab131366), was used for detection at 1/1500 dilution.
Lane 1 : HeLa whole cell lysate 10ug (Input). Lane 2 : ab200663 IP in HeLa whole cell lysate. Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab200663 in HeLa whole cell lysate.
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 3 min (Panel A); 10 seconds (Panel B).
All lanes:
Immunoprecipitation - Anti-CSDE1/NRU antibody [EPR17413] (<a href='/en-us/products/primary-antibodies/csde1-nru-antibody-epr17413-ab200663'>ab200663</a>)
Predicted band size: 89 kDa
false
- IP
Supplier Data
Immunoprecipitation - Anti-CSDE1/NRU antibody [EPR17413] - BSA and Azide free (AB251319)
This data was developed using ab200663, the same antibody clone in a different buffer formulation.
CSDE1/NRU was immunoprecipitated from 1mg of HeLa (Human epithelial cells from cervix adenocarcinoma) whole cell lysate with ab200663 at 1/140 dilution. Western blot was performed from the immunoprecipitate using ab200663 at 1/5000 dilution. Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG, was used as secondary antibody at 1/1500 dilution.
Lane 1 : HeLa whole cell lysate 10ug (Input). Lane 2 : ab200663 IP in HeLa whole cell lysate. Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab200663 in HeLa whole cell lysate.
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 30 seconds.
All lanes:
Immunoprecipitation - Anti-CSDE1/NRU antibody [EPR17413] (<a href='/en-us/products/primary-antibodies/csde1-nru-antibody-epr17413-ab200663'>ab200663</a>)
Predicted band size: 89 kDa,93 kDa
false
- WB
Supplier Data
Western blot - Anti-CSDE1/NRU antibody [EPR17413] - BSA and Azide free (AB251319)
This data was developed using ab200663, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-CSDE1/NRU antibody [EPR17413] (<a href='/en-us/products/primary-antibodies/csde1-nru-antibody-epr17413-ab200663'>ab200663</a>) at 1/2000 dilution
Lane 1:
K562 (Human chronic myelogenous leukemia cells from bone marrow) cell lysate at 20 µg
Lane 2:
HeLa (Human epithelial cells from cervix adenocarcinoma) cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 89 kDa
Observed band size: 89 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-CSDE1/NRU antibody [EPR17413] - BSA and Azide free (AB251319)
This data was developed using ab200663, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-CSDE1/NRU antibody [EPR17413] (<a href='/en-us/products/primary-antibodies/csde1-nru-antibody-epr17413-ab200663'>ab200663</a>) at 1/1000 dilution
All lanes:
MCF-7 (Human breast adenocarcinoma cell line) cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 89 kDa
Observed band size: 89 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-CSDE1/NRU antibody [EPR17413] - BSA and Azide free (AB251319)
This data was developed using ab200663, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
The HeLa cell fractions lysate set is ab168542 from Abcam.
All lanes:
Western blot - Anti-CSDE1/NRU antibody [EPR17413] (<a href='/en-us/products/primary-antibodies/csde1-nru-antibody-epr17413-ab200663'>ab200663</a>) at 1/2000 dilution
Lane 1:
HeLa cytosolic fraction at 10 µg
Lane 2:
HeLa membrane (mitochondrial) fraction at 10 µg
Lane 3:
HeLa nuclear fraction at 10 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/50000 dilution
Predicted band size: 89 kDa
Observed band size: 89 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-CSDE1/NRU antibody [EPR17413] - BSA and Azide free (AB251319)
This data was developed using ab200663, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-CSDE1/NRU antibody [EPR17413] (<a href='/en-us/products/primary-antibodies/csde1-nru-antibody-epr17413-ab200663'>ab200663</a>) at 1/1000 dilution
All lanes:
Human fetal brain tissue lysate at 10 µg
Secondary
All lanes:
Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG at 1/1000 dilution
Predicted band size: 89 kDa
Observed band size: 89 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-CSDE1/NRU antibody [EPR17413] - BSA and Azide free (AB251319)
This data was developed using ab200663, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-CSDE1/NRU antibody [EPR17413] (<a href='/en-us/products/primary-antibodies/csde1-nru-antibody-epr17413-ab200663'>ab200663</a>) at 1/1000 dilution
Lane 1:
C6 (Rat glial tumor cells) cell lysate at 10 µg
Lane 2:
RAW 264.7 (Mouse macrophage cells transformed with Abelson murine leukemia virus) cell lysate at 10 µg
Lane 3:
PC-12 (Rat adrenal gland pheochromocytoma) cell lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 89 kDa
Observed band size: 89 kDa
false
Exposure time: 1min
Related conjugates and formulations (1)
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Anti-CSDE1/NRU antibody [EPR17413]
Reactivity data
Product details
ab251319 is the carrier-free version of ab200663.
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.
Properties and storage information
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Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Storage information
Product protocols
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Target data
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