Anti-CEP290 antibody [EPR28924-76]
- 20ul selling size
- Recombinant
- RabMAb
- What is this?
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Rabbit Recombinant Monoclonal CEP290 antibody. Suitable for WB, ICC/IF and reacts with Human, Mouse samples.
View Alternative Names
BBS14, KIAA0373, NPHP6, CEP290, Centrosomal protein of 290 kDa, Cep290, Bardet-Biedl syndrome 14 protein, Cancer/testis antigen 87, Nephrocystin-6, Tumor antigen se2-2, CT87
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-CEP290 antibody [EPR28924-76] (AB318278)
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized HeLa (human cervical adenocarcinoma epithelial cell) cells labelling CEP290 with ab318278 at 1/50 (10.38 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2 ug/mL dilution (Green).
Confocal image showing positive staining on the centrosome in HeLa cell line (shown in green). The counterstain was observed in magenta. Nuclear DNA was labeled with DAPI (shown in blue). 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 (Magenta). 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 2 ug/mL dilution.
- WB
Supplier Data
Western blot - Anti-CEP290 antibody [EPR28924-76] (AB318278)
The high-sensitivity ECL substrate allows for the detection of proteins in the mid-femtogram range.
In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) staining at 1/10000 dilution.
All lanes:
Western blot - Anti-CEP290 antibody [EPR28924-76] (ab318278) at 1/1000 dilution
Lane 1:
Human placenta tissue lysate at 50 µg
Lane 2:
Human adrenal gland tissue lysate at 50 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 290 kDa,124 kDa
true
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-CEP290 antibody [EPR28924-76] (AB318278)
The lane 4 was developed using a high sensitivity ECL substrate. The high-sensitivity ECL substrate allows for the detection of proteins in the mid-femtogram range.
In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) staining at 1/10000 dilution.
Exposure time : Lanes 1-3 : 92 seconds, lane 4 : 180 seconds
All lanes:
Western blot - Anti-CEP290 antibody [EPR28924-76] (ab318278) at 1/1000 dilution
Lane 1:
HeLa (human cervical adenocarcinoma epithelial cell) transfected with scrambled siRNA control whole cell lysate at 20 µg
Lane 2:
HeLa transfected with siRNA specifically targeting CEP290 whole cell lysate at 20 µg
Lane 3:
K-562 (human chronic myelogenous leukemia lymphoblast) whole cell lysate at 40 µg
Lane 4:
Hepa1-6 (mouse hepatoma epithelial cell) whole cell lysate at 40 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 1/100000 dilution
Observed band size: 290 kDa,124 kDa
false
- WB
Supplier Data
Western blot - Anti-CEP290 antibody [EPR28924-76] (AB318278)
The high-sensitivity ECL substrate allows for the detection of proteins in the mid-femtogram range.
Low expression : skeletal muscle.
The identity of the bands between 130 kDa and 250 kDa are unknown.
In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) staining at 1/10000 dilution.
All lanes:
Western blot - Anti-CEP290 antibody [EPR28924-76] (ab318278) at 1/1000 dilution
Lane 1:
Mouse olfactory bulb tissue lysate at 50 µg
Lane 2:
Mouse brain tissue lysate at 50 µg
Lane 3:
Mouse skeletal muscle lysate at 50 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 1/20000 dilution
Observed band size: 290 kDa,124 kDa
true
Exposure time: 180s
Related conjugates and formulations (1)
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Anti-CEP290 antibody [EPR28924-76] - BSA and Azide free
Reactivity data
Product details
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
CEP290 contributes significantly to the formation and maintenance of the primary cilium a cellular organelle. It forms part of the transition zone complex a critical region at the base of cilia. This zone functions as a barrier regulating the movement of molecules in and out of the cilia. As a result CEP290 supports the transport and localization of ciliary proteins affecting ciliary homeostasis and signal transduction mechanisms within the cell.
Pathways
CEP290 is intricately involved in the ciliary transport and the phototransduction pathway within photoreceptor cells. CEP290 operates in coordination with proteins such as RPGR in these pathways ensuring proper ciliary trafficking and function. This activity is important for sensory perception processes including vision. The disruption of CEP290 affects these pathways leading to compromised sensory functions.
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'.
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