Anti-IL-16 antibody [EPR19988] - BSA and Azide free
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal IL-16 antibody. Carrier free. Suitable for ICC/IF, IP, WB, Flow Cyt (Intra), IHC-P and reacts with Human samples.
View Alternative Names
Pro-interleukin-16, IL16
- WB
Supplier Data
Western blot - Anti-IL-16 antibody [EPR19988] - BSA and Azide free (AB251467)
This data was developed using ab207181, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
Exposure times : Lane 1 : 5 seconds, Lane 2 : 15 seconds, Lane 3 : 3 minutes.
The band at 80 kDa is pro-IL-16 and the bands at 40-75 kDa are cleaved fragments. This is consistent with what has been described in the literature (PMID : 15187155; 9144227; 9743378; 14734747).
All lanes:
Western blot - Anti-IL-16 antibody [EPR19988] (<a href='/en-us/products/primary-antibodies/il-16-antibody-epr19988-ab207181'>ab207181</a>) at 1/1000 dilution
Lane 1:
Human thymus tissue lysate at 10 µg
Lane 2:
Human spleen tissue lysate at 10 µg
Lane 3:
Human tonsil tissue lysate at 20 µg
Secondary
Lanes 1 - 2:
Western blot - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/4000 dilution
Lane 3:
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
Predicted band size: 142 kDa
Observed band size: 75-40 kDa,80 kDa
false
- WB
Supplier Data
Western blot - Anti-IL-16 antibody [EPR19988] - BSA and Azide free (AB251467)
This data was developed using ab207181, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
The band at 80 kDa is pro-IL-16 and the bands at 40-75 kDa are cleaved fragments. This is consistent with what has been described in the literature (PMID : 15187155, 9144227, 9743378, 14734747).
All lanes:
Western blot - Anti-IL-16 antibody [EPR19988] (<a href='/en-us/products/primary-antibodies/il-16-antibody-epr19988-ab207181'>ab207181</a>) at 1/1000 dilution
Lane 1:
H9 (Human cutaneous T lymphocyte lymphoma cell line) whole cell lysate at 10 µg
Lane 2:
Jurkat (Human T cell leukemia cell line from peripheral blood) whole cell lysate at 10 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
Predicted band size: 142 kDa
Observed band size: 75-40 kDa,80 kDa
false
Exposure time: 3min
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IL-16 antibody [EPR19988] - BSA and Azide free (AB251467)
This data was developed using ab207181, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human tonsil tissue labeling IL-16 with ab207181 at 1/2000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution. Cytoplasmic staining on human tonsil is observed [PMID : 10946273]. Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-IL-16 antibody [EPR19988] - BSA and Azide free (AB251467)
This data was developed using ab207181, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized H9 (Human cutaneous T lymphocyte lymphoma cell line) cells labeling IL-16 with ab207181 at 1/100 dilution, followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (green). Confocal image showing cytoplasmic staining on H9 cell line.
The nuclear counter stain is DAPI (blue). Tubulin is detected with ab195889 (Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594)) at 1/200 dilution (red).
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) at 1/1000 dilution.
- IP
Supplier Data
Immunoprecipitation - Anti-IL-16 antibody [EPR19988] - BSA and Azide free (AB251467)
This data was developed using ab207181, the same antibody clone in a different buffer formulation.
IL-16 was immunoprecipitated from 0.35 mg of H9 (Human cutaneous T lymphocyte lymphoma cell line) whole cell lysate with ab207181 at 1/30 dilution. Western blot was performed from the immunoprecipitate using ab207181 at 1/1000 dilution. VeriBlot for IP Detection Reagent (HRP) (ab131366), was used for detection at 1/10000 dilution.
Lane 1 : H9 whole cell lysate, 10 μg (Input).
Lane 2 : ab207181 IP in H9 whole cell lysate.
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab207181 in H9 whole cell lysate.
Blocking and dilution buffer : 5% NFDM/TBST.
Exposure time : 10 seconds.
Note : The band at around 50kDa is a cleaved form of IL-16.
All lanes:
Immunoprecipitation - Anti-IL-16 antibody [EPR19988] (<a href='/en-us/products/primary-antibodies/il-16-antibody-epr19988-ab207181'>ab207181</a>)
Predicted band size: 142 kDa
Observed band size: 37-80 kDa
false
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-IL-16 antibody [EPR19988] - BSA and Azide free (AB251467)
This data was developed using ab207181, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human colon tissue labeling IL-16 with ab207181 at 1/2000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution. Cytoplasmic staining on stromal cells of human colon is observed [PMID : 11709514]. Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-IL-16 antibody [EPR19988] - BSA and Azide free (AB251467)
This data was developed using ab207181, the same antibody clone in a different buffer formulation.
Intracellular flow cytometric analysis of 4% paraformaldehyde-fixed H9 (Human cutaneous T lymphocyte lymphoma cell line) cells labeling IL-16 with ab207181 at 1/600 dilution (red) compared with a rabbit monoclonal IgG isotype control (ab172730; black) and an unlabeled control (cells without incubation with primary antibody and secondary antibody; blue). Goat anti rabbit IgG (Alexa Fluor® 488) at 1/2000 dilution was used as the secondary antibody.
Related conjugates and formulations (1)
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Anti-IL-16 antibody [EPR19988]
Reactivity data
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Why is this recommended?
We recommend this product because it’s often used in the same experiment or related research.
We advise that you always check the datasheet to ensure it fits your experiments, or contact ourtechnical teamfor help.
Product details
ab251467 is the carrier-free version of ab207181.
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.
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