Anti-CLEC14A antibody [EPR30282-549] - BSA and Azide free
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal CLEC14A antibody. Carrier free. Suitable for Flow Cyt, IHC-P, WB and reacts with Mouse samples.
View Alternative Names
C-type lectin domain family 14 member A, Clec14a
- Flow Cyt
Lab
Flow Cytometry - Anti-CLEC14A antibody [EPR30282-549] - BSA and Azide free (AB326428)
This data was developed using ab326425, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of bEnd.3 (mouse brain endothelial cell, Right) EL4 (mouse lymphoma T lymphocyte, Left) cells labelling CLEC14A with ab326425 at 1/50 dilution (1ug) / Red compared with a Rabbit monoclonal IgG (ab172730) / Black isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody).
Goat anti-Rabbit IgG (Alexa Fluor® 647, ab150083) at 1/5000 dilution was used as the secondary antibody.
Gated on viable cells. Negative control : EL4
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CLEC14A antibody [EPR30282-549] - BSA and Azide free (AB326428)
This data was developed using ab326425, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse squamous cell carcinoma tissue labeling CLEC14A with ab326425 at 1/500 (0.994 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on endothelial cells of mouse squamous cell carcinoma.
The primary antibody was incubated 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
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CLEC14A antibody [EPR30282-549] - BSA and Azide free (AB326428)
This data was developed using ab326425, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded (A) bEnd.3 (mouse brain endothelial cell) cell pellet (B) EL4 (mouse lymphoma T lymphocyte) cell pellet tissue labeling CLEC14A with ab326425 at 1/200 (2.485 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on (A) bEnd.3 cell pellet, no staining on (B) EL4 cell pellet.
The primary antibody was incubated 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
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CLEC14A antibody [EPR30282-549] - BSA and Azide free (AB326428)
This data was developed using ab326425, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse pancreas tissue labeling CLEC14A with ab326425 at 1/500 (0.994 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on endothelial cells of mouse pancreas.
The primary antibody was incubated 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
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CLEC14A antibody [EPR30282-549] - BSA and Azide free (AB326428)
This data was developed using ab326425, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse lung tissue labeling CLEC14A with ab326425 at 1/500 (0.994 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on endothelial cells of mouse lung.
The primary antibody was incubated 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
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CLEC14A antibody [EPR30282-549] - BSA and Azide free (AB326428)
This data was developed using ab326425, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labeling CLEC14A with ab326425 at 1/500 (0.994 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Low expression tissue : Weak staining on endothelial cells of mouse cerebrum.
The primary antibody was incubated 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
- WB
Lab
Western blot - Anti-CLEC14A antibody [EPR30282-549] - BSA and Azide free (AB326428)
This data was developed using ab326425, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Low expression : liver, brain, skeletal muscle.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) (1 : 200000) (36KDa).
All lanes:
Western blot - Anti-CLEC14A antibody [EPR30282-549] (<a href='/en-us/products/primary-antibodies/clec14a-antibody-epr30282-549-ab326425'>ab326425</a>) at 1/1000 dilution
Lane 1:
Mouse lung tissue lysate at 20 µg
Lane 2:
Mouse liver tissue lysate at 20 µg
Lane 3:
Mouse brain tissue lysate at 20 µg
Lane 4:
Mouse skeletal 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 1/100000 dilution
Observed band size: 100 kDa,36 kDa
false
Exposure time: 180s
- WB
Lab
Western blot - Anti-CLEC14A antibody [EPR30282-549] - BSA and Azide free (AB326428)
This data was developed using ab326425, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Negative control : EL4, NIH/3T3.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 21706054).
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) (1 : 200000) (36KDa).
All lanes:
Western blot - Anti-CLEC14A antibody [EPR30282-549] (<a href='/en-us/products/primary-antibodies/clec14a-antibody-epr30282-549-ab326425'>ab326425</a>) at 1/1000 dilution
Lane 1:
bEnd.3 (mouse brain endothelial cell) whole cell lysate at 20 µg
Lane 2:
EL4 (mouse lymphoma T lymphocyte) whole cell lysate at 20 µg
Lane 3:
NIH/3T3 (mouse embryonic fibroblast) whole cell 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: 100 kDa,36 kDa
false
Exposure time: 59s
Reactivity data
Product details
ab326428 is the carrier-free version of ab326425
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
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
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