Anti-HLA-C antibody [EPR26121-73] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal HLAC antibody. Carrier free. Suitable for IP, IHC-P, WB and reacts with Human, Transfected cell lysate - Human samples.
View Alternative Names
HLAC, HLA-C, HLA-Cw, Human leukocyte antigen C
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-HLA-C antibody [EPR26121-73] - BSA and Azide free (AB307362)
This data was developed using ab307361, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human tonsil tissue labeling HLA-C with ab307361 at 1/4000 (0.126 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection) was used. Positive staining on human tonsil (PMID : 17008885). The section was incubated with ab307361 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) was used. Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 10 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-HLA-C antibody [EPR26121-73] - BSA and Azide free (AB307362)
This data was developed using ab307361, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human NKT lymphoma tissue labeling HLA-C with ab307361 at 1/4000 (0.126 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection) was used. Positive staining on NKT lymphoma. The section was incubated with ab307361 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) was used. Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 10 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-HLA-C antibody [EPR26121-73] - BSA and Azide free (AB307362)
This data was developed using ab307361, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human colon tissue labeling HLA-C with ab307361 at 1/4000 (0.126 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection) was used. Positive staining on human colon (PMID : 17008885). The section was incubated with ab307361 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) was used. Heat mediated antigen retrieval was performed with Citrate buffer (pH 6.0, Epitope Retrieval Solution 1) for 10 mins
- IP
Supplier Data
Immunoprecipitation - Anti-HLA-C antibody [EPR26121-73] - BSA and Azide free (AB307362)
This data was developed using ab307361, the same antibody clone in a different buffer formulation. HLA-C was immunoprecipitated from 0.35 mg Jurkat whole cell lysate with ab307361 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab307361 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution. Lane 1 : Jurkat (human T cell leukemia T lymphocyte) whole cell lysate Lane 2 : ab307361 IP in Jurkat whole cell lysate Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab307361 in Jurkat whole cell lysate Blocking and dilution buffer and concentration : 5% NFDM/TBST. Exposure time : 10 seconds
All lanes:
Immunoprecipitation - Anti-HLA-C antibody [EPR26121-73] (<a href='/en-us/products/primary-antibodies/hla-c-antibody-epr26121-73-ab307361'>ab307361</a>) at 1/30 dilution
All lanes:
Jurkat (human T cell leukemia T lymphocyte) whole cell lysate
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
false
Exposure time: 10s
- WB
Supplier Data
Western blot - Anti-HLA-C antibody [EPR26121-73] - BSA and Azide free (AB307362)
This data was developed using ab307361, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST Exposure time : 26 seconds
All lanes:
Western blot - Anti-HLA-C antibody [EPR26121-73] (<a href='/en-us/products/primary-antibodies/hla-c-antibody-epr26121-73-ab307361'>ab307361</a>) at 1/1000 dilution
Lane 1:
Jurkat (human T cell leukemia T lymphocyte) transfected with scrambled siRNA control whole cell lysate at 20 µg
Lane 2:
Jurkat transfected with siRNA specifically targeti HLA-C 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 1/100000 dilution
Observed band size: 41 kDa
false
Exposure time: 26s
- WB
Supplier Data
Western blot - Anti-HLA-C antibody [EPR26121-73] - BSA and Azide free (AB307362)
This data was developed using ab307361, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST Exposure time : 7.25 seconds
All lanes:
Western blot - Anti-HLA-C antibody [EPR26121-73] (<a href='/en-us/products/primary-antibodies/hla-c-antibody-epr26121-73-ab307361'>ab307361</a>) at 1/1000 dilution
All lanes:
Human colon tissue lysate at 40 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 41 kDa
false
Exposure time: 7.25s
- WB
Supplier Data
Western blot - Anti-HLA-C antibody [EPR26121-73] - BSA and Azide free (AB307362)
This data was developed using ab307361, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST Exposure time : 15 seconds
All lanes:
Western blot - Anti-HLA-C antibody [EPR26121-73] (<a href='/en-us/products/primary-antibodies/hla-c-antibody-epr26121-73-ab307361'>ab307361</a>) at 1/1000 dilution
Lane 1:
Jurkat (human T cell leukemia T lymphocyte) whole cell lysate at 80 µg
Lane 2:
A375 (human malignant melanoma epithelial cell) whole cell lysate at 80 µg
Lane 3:
HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate at 80 µg
Lane 4:
Human lymphoma tissue lysate at 80 µg
Lane 5:
HL-60 (human acute promyelocytic leukemia promyeloblast) whole cell lysate at 80 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: 41 kDa
false
Exposure time: 15s
- WB
Supplier Data
Western blot - Anti-HLA-C antibody [EPR26121-73] - BSA and Azide free (AB307362)
This data was developed using ab307361, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST This antibody does not cross-react with human HLA-A and HLA-B. Exposure time : 3.25 seconds
All lanes:
Western blot - Anti-HLA-C antibody [EPR26121-73] (<a href='/en-us/products/primary-antibodies/hla-c-antibody-epr26121-73-ab307361'>ab307361</a>) at 1/1000 dilution
Lane 1:
HEK-293T cells transfected with an empty vector containi a his tag whole cell lysate at 20 µg
Lane 2:
HEK-293T cells transfected with a human HLA-C expression vector containi a his tag whole cell lysate at 20 µg
Lane 3:
HEK-293T cells transfected with a human HLA-A expression vector containi a his tag whole cell lysate at 20 µg
Lane 4:
HEK-293T cells transfected with a human HLA-B expression vector containi a his tag 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 1/100000 dilution
Observed band size: 41 kDa
false
Exposure time: 3.25s
Related conjugates and formulations (1)
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Anti-HLA-C antibody [EPR26121-73]
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.
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