Anti-CXCL11 antibody [EPR27375-62] - BSA and Azide free
- RabMAb
- Recombinant
- BOND RX™ Validated
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Rabbit Recombinant Monoclonal CXCL11 antibody. Carrier free. Suitable for IHC-P and reacts with Transfected cell line - Human, Human samples.
View Alternative Names
ITAC, SCYB11, SCYB9B, CXCL11, C-X-C motif chemokine 11, Beta-R1, H174, Interferon gamma-inducible protein 9, Interferon-inducible T-cell alpha chemoattractant, Small-inducible cytokine B11, IP-9, I-TAC
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CXCL11 antibody [EPR27375-62] - BSA and Azide free (AB326599)
This data was developed using ab322902, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Panel A HEK-293T cells transfected with a CXCL11 expression vector containing a his tag, Panel B HEK-293T cells transfected with a CXCL9 expression vector containing a his tag, Panel C HEK-293T cells transfected with a CXCL10 expression vector containing a his tag, Panel D HEK-293T cells transfected with a CXCL2 expression vector containing a his tag and Panel E HEK-293T cells transfected with empty vector containing a his tag labeling CXCL11 with ab322902 at 1/2000 (0.259 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on (A) HEK-293T transfected with a CXCL11 expression vector, no staining on (B) HEK-293T transfected with a CXCL9 expression vector, (C) HEK-293T transfected with a CXCL10 expression vector, (D) HEK-293T transfected with a CXCL2 expression vector, and (E) HEK-293T transfected with empty vector.
The section was incubated with ab322902 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-CXCL11 antibody [EPR27375-62] - BSA and Azide free (AB326599)
This data was developed using ab322902, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human prostate cancer tissue labeling CXCL11 with ab322902 at 1/100 (5.17 ug/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human prostate cancer.
The section was incubated with ab322902 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-CXCL11 antibody [EPR27375-62] - BSA and Azide free (AB326599)
This data was developed using ab322902, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Panel A untreated THP-1 cells, Panel B THP-1 cells treated with a combination of IFN-γ (200ng/ml, 24h) and LPS (50ng/ml, 24h) and Panel C THP-1 cells treated with a combination of IFN-γ (200ng/ml 16h+8h), LPS (50ng/ml 16h+8h) add BFA (300ng/ml 8h) labeling CXCL11 with ab322902 at 1/20 (25.85 ug/ml) dilution, followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP).
Positive staining on (C) THP-1 cells treated with a combination of IFN-γ, LPS add BFA; weak staining on (B) THP-1 cells treated with a combination of IFN-γ and LPS; no staining on (A) untreated THP-1 cells.
The section was incubated with ab322902 at 4°C overnight.
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP).
Heat mediated antigen retrieval was performed using ab93684 (Tris/EDTA buffer, pH 9.0)
Related conjugates and formulations (1)
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Anti-CXCL11 antibody [EPR27375-62]
Reactivity data
Product details
ab326599 is the carrier-free version of ab322902
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
- Visit the General 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