Anti-DCTN1/p150-glued antibody [EPR26464-28] (BSA and Azide free)
- BOND RX™ Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal DCTN1/p150-glued antibody. Carrier free. Suitable for IP, Flow Cyt (Intra), ICC/IF, IHC-Fr, IHC-P, WB and reacts with Mouse, Human samples.
View Alternative Names
Dynactin subunit 1, 150 kDa dynein-associated polypeptide, DAP-150, p135, p150-glued, DP-150, DCTN1
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-DCTN1/p150-glued antibody [EPR26464-28] (BSA and Azide free) (AB302630)
This data was developed using ab302629, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized HeLa (human cervix adenocarcinoma epithelial cell) labelling DCTN1/p150-glued with ab302629 at 1/200 (9.955 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 cytoplasm staining in HeLa cell line (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue). Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
ab7291 Anti-alpha Tubulin antibody [DM1A] - Loading Control was used to counterstain tubulin at 1/1000 (1 ug/ml) dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
-ve control 1 : ab302629 at 1/50 dilution, followed by ab150120 Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) antibody at 1/1000 dilution.
-ve control 2 : ab7291 at 1/1000 dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution.
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-DCTN1/p150-glued antibody [EPR26464-28] (BSA and Azide free) (AB302630)
This data was developed using ab302629, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized HeLa (human cervix adenocarcinoma epithelial cell) cells labelling DCTN1/p150-glued with ab302629 at 1/2000 (Red) compared with a Rabbit IgG, monoclonal [EPR25A] - Isotype Control (ab172730) (Black) . Unlabelled control (cells without incubation with primary antibody and secondary antibody) / Blue.
- IP
Lab
Immunoprecipitation - Anti-DCTN1/p150-glued antibody [EPR26464-28] (BSA and Azide free) (AB302630)
This data was developed using ab302629, the same antibody clone in a different buffer formulation
DCTN1/p150-glued was immunoprecipitated from 0.35 mg HeLa whole cell lysate with ab302629 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab302629 at 1/1000 dilution.
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
All lanes:
Immunoprecipitation - Anti-DCTN1/p150-glued antibody [EPR26464-28] (<a href='/en-us/products/primary-antibodies/dctn1-p150-glued-antibody-epr26464-28-ab302629'>ab302629</a>) at 1/1000 dilution
Lane 1:
HeLa (human cervix adenocarcinoma epithelial cell), whole cell lysate at 10 µg
Lane 2:
<a href='/en-us/products/primary-antibodies/dctn1-p150-glued-antibody-epr26464-28-ab302629'>ab302629</a> at 1/30 IP in HeLa whole cell lysate at 10 µg
Lane 3:
Rabbit monoclonal IgG (<a href='/en-us/products/primary-antibodies/rabbit-igg-monoclonal-epr25a-isotype-control-ab172730'>ab172730</a>) instead of <a href='/en-us/products/primary-antibodies/dctn1-p150-glued-antibody-epr26464-28-ab302629'>ab302629</a> in HeLa whole cell lysate at 10 µg
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
Observed band size: 150 kDa
false
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-DCTN1/p150-glued antibody [EPR26464-28] (BSA and Azide free) (AB302630)
This data was developed using ab302629, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized Neuro-2a (mouse neuroblastoma neuroblast) cells labelling DCTN1/p150-glued with ab302629 at 1/200 (9.955 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 cytoplasm staining in Neuro-2a cell line (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue). Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
ab7291 Anti-alpha Tubulin antibody [DM1A] - Loading Control was used to counterstain tubulin at 1/1000 (1 ug/ml) dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
-ve control 1 : ab302629 at 1/50 dilution, followed by ab150120 Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) antibody at 1/1000 dilution.
-ve control 2 : ab7291 at 1/1000 dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution.
- IHC-Fr
Lab
Immunohistochemistry (Frozen sections) - Anti-DCTN1/p150-glued antibody [EPR26464-28] (BSA and Azide free) (AB302630)
This data was developed using ab302629, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen mouse liver (fresh) tissue labelling DCTN1/p150-glued with ab302629 at 1/100 (19.91 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green).
Negative control : no staining on mouse liver (PMID : 1836789).
The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 2 ug/mL dilution.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-DCTN1/p150-glued antibody [EPR26464-28] (BSA and Azide free) (AB302630)
This data was developed using ab302629, the same antibody clone in a different buffer formulation. Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Neuro-2a (mouse neuroblastoma neuroblast) cells labelling DCTN1/p150-glued with ab302629 at 1/50 dilution (1ug) (Red) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-DCTN1/p150-glued antibody [EPR26464-28] (BSA and Azide free) (AB302630)
This data was developed using ab302629, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse dorsal root ganglion tissue labelling DCTN1/p150-glued with ab302629 at 1/3500 dilution.
Positive staining on mouse dorsal root ganglion.
The section was incubated with ab302629 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Heat mediated antigen retrieval using Bond™ Epitope Retrieval Solution 2 (pH 9.0) for 20 mins.
- IHC-Fr
Lab
Immunohistochemistry (Frozen sections) - Anti-DCTN1/p150-glued antibody [EPR26464-28] (BSA and Azide free) (AB302630)
This data was developed using ab302629, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse spinal cord (fresh) tissue labelling DCTN1/p150-glued with ab302629 at 1/100 (19.91 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/mL) dilution (Green).
Confocal image showing positive staining on mouse spinal cord. The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-DCTN1/p150-glued antibody [EPR26464-28] (BSA and Azide free) (AB302630)
This data was developed using ab302629, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse cerebrum labelling DCTN1/p150-glued with ab302629 at 1/3500 dilution.
Positive staining on mouse cerebrum.
The section was incubated with ab302629 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Heat mediated antigen retrieval using Bond™ Epitope Retrieval Solution 2 (pH 9.0) for 20 mins.
- IP
Lab
Immunoprecipitation - Anti-DCTN1/p150-glued antibody [EPR26464-28] (BSA and Azide free) (AB302630)
This data was developed using ab302629, the same antibody clone in a different buffer formulation.
DCTN1/p150-glued was immunoprecipitated from 0.35 mg mouse Neuro-2a whole cell lysate with ab302629 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab302629 at 1/1000 dilution.
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
All lanes:
Immunoprecipitation - Anti-DCTN1/p150-glued antibody [EPR26464-28] (<a href='/en-us/products/primary-antibodies/dctn1-p150-glued-antibody-epr26464-28-ab302629'>ab302629</a>) at 1/1000 dilution
Lane 1:
Neuro-2a (mouse neuroblastoma neuroblast), whole cell lysate at 10 µg
Lane 2:
<a href='/en-us/products/primary-antibodies/dctn1-p150-glued-antibody-epr26464-28-ab302629'>ab302629</a> at 1/30 IP in Neuro-2a whole cell lysate at 10 µg
Lane 3:
Rabbit monoclonal IgG (<a href='/en-us/products/primary-antibodies/rabbit-igg-monoclonal-epr25a-isotype-control-ab172730'>ab172730</a>) instead of <a href='/en-us/products/primary-antibodies/dctn1-p150-glued-antibody-epr26464-28-ab302629'>ab302629</a> in Neuro-2a whole cell lysate at 10 µg
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
Observed band size: 150 kDa
false
Exposure time: 180s
- WB
Lab
Western blot - Anti-DCTN1/p150-glued antibody [EPR26464-28] (BSA and Azide free) (AB302630)
This data was developed using ab302629, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
All lanes:
Western blot - Anti-DCTN1/p150-glued antibody [EPR26464-28] (<a href='/en-us/products/primary-antibodies/dctn1-p150-glued-antibody-epr26464-28-ab302629'>ab302629</a>) at 1/1000 dilution
Lane 1:
HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 2:
SH-SY5Y (human neuroblastoma epithelial cell) whole cell lysate at 20 µg
Lane 3:
Neuro-2a (mouse neuroblastoma neuroblast) whole cell lysate at 20 µg
Lane 4:
NIH/3T3 (mouse embryonic fibroblast) whole cell lysate at 20 µg
Lane 5:
Mouse brain tissue lysate at 20 µg
Lane 6:
Mouse cerebellum tissue lysate at 20 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: 150 kDa
false
Exposure time: 20s
Reactivity data
Product details
Want a custom formulation?
This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com
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.
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.
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.
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Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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