Anti-TRAF1 antibody [EPR26204-112] (BSA and Azide free)
- BOND RX™ Validated
- RabMAb
- Recombinant
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(1 Publication)
Rabbit Recombinant Monoclonal TRAF1 antibody. Carrier free. Suitable for WB, IP, IHC-P and reacts with Human, Rat, Mouse samples. Cited in 1 publication.
View Alternative Names
EBI6, TRAF1, TNF receptor-associated factor 1, Epstein-Barr virus-induced protein 6
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TRAF1 antibody [EPR26204-112] (BSA and Azide free) (AB300076)
This data was developed using ab300075, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human thymus tissue labelling TRAF1 with ab300075 at 1/1000 (0.564 μg/ml) followed by a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) kit. Cytoplasmic staining on human thymus (PMID : 11046039). The section was incubated with ab300075 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 Leica DS9800 (BOND™ Polymer Refine Detection) kit.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TRAF1 antibody [EPR26204-112] (BSA and Azide free) (AB300076)
This data was developed using ab300075, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human Hodgkin's lymphoma tissue labelling TRAF1 with ab300075 at 1/1000 (0.564 µg/ml) followed by a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) was used. Cytoplasmic staining on Reed-Sternberg cells in human Hodgkin's lymphoma (PMID : 12502848). The section was incubated with ab300075 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 Leica DS9800 (BOND™ Polymer Refine Detection) kit. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TRAF1 antibody [EPR26204-112] (BSA and Azide free) (AB300076)
This data was developed using ab300075, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human thymus tissue labelling TRAF1 with ab300075 at 1/1000 (0.564 µg/ml) followed by a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) kit. Cytoplasmic staining on human thymus (PMID : 11046039). The section was incubated with ab300075 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 Leica DS9800 (BOND™ Polymer Refine Detection) kit. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TRAF1 antibody [EPR26204-112] (BSA and Azide free) (AB300076)
This data was developed using ab300075, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human lymph node hyperplasia tissue labelling TRAF1 with ab300075 at 1/1000 (0.564 µg/ml) followed by a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) kit. Cytoplasmic staining on human lymph node hyperplasia (PMID : 11046039). The section was incubated with ab300075 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 Leica DS9800 (BOND™ Polymer Refine Detection) was used. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TRAF1 antibody [EPR26204-112] (BSA and Azide free) (AB300076)
This data was developed using ab300075, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human Hodgkin's lymphoma tissue labelling TRAF1 with ab300075 at 1/1000 (0.564 μg/ml) followed by a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) was used. Cytoplasmic staining on Reed-Sternberg cells in human Hodgkin's lymphoma (PMID : 12502848). The section was incubated with ab300075 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 Leica DS9800 (BOND™ Polymer Refine Detection) kit.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TRAF1 antibody [EPR26204-112] (BSA and Azide free) (AB300076)
This data was developed using ab300075, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human lymph node hyperplasia tissue labelling TRAF1 with ab300075 at 1/1000 (0.564 μg/ml) followed by a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) kit. Cytoplasmic staining on human lymph node hyperplasia (PMID : 11046039). The section was incubated with ab300075 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 Leica DS9800 (BOND™ Polymer Refine Detection) was used.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins
- IP
Supplier Data
Immunoprecipitation - Anti-TRAF1 antibody [EPR26204-112] (BSA and Azide free) (AB300076)
This data was developed using ab300075, the same antibody clone in a different buffer formulation. TRAF1 was immunoprecipitated from 0.35 mg Raji (human Burkitt's lymphoma B lymphocyte) whole cell lysate 10 µg with ab300075 at 1/30 dilution (2µg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab300075 at 1/1000 dilution. VeriBlot for IP secondary antibody (HRP)(ab131366) was used at 1/5000 dilution. Lane 1 : Raji (human Burkitt's lymphoma B lymphocyte) whole cell lysate 10 µg Lane 2 : ab300075 in Raji whole cell lysate Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab300075 in Raji whole cell lysate Blocking and dilution buffer and concentration : 5% NFDM/TBST. Exposure time : 10 seconds
All lanes:
Immunoprecipitation - Anti-TRAF1 antibody [EPR26204-112] (<a href='/en-us/products/primary-antibodies/traf1-antibody-epr26204-112-ab300075'>ab300075</a>) at 1/1000 dilution
All lanes:
Raji (human Burkitt's lymphoma B 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
Predicted band size: 46 kDa
Observed band size: 50 kDa
false
Exposure time: 10s
- IP
Supplier Data
Immunoprecipitation - Anti-TRAF1 antibody [EPR26204-112] (BSA and Azide free) (AB300076)
This data was developed using ab300075, the same antibody clone in a different buffer formulation.
TRAF1 was immunoprecipitated from 0.35 mg Raji (human Burkitt's lymphoma B lymphocyte) whole cell lysate 10 μg with ab300075 at 1/30 dilution (2μg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab300075 at 1/1000 dilution. VeriBlot for IP secondary antibody (HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : Raji (human Burkitt's lymphoma B lymphocyte) whole cell lysate 10 μg
Lane 2 : ab300075 in Raji whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab300075 in Raji whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 10 seconds
All lanes:
Immunoprecipitation - Anti-TRAF1 antibody [EPR26204-112] (<a href='/en-us/products/primary-antibodies/traf1-antibody-epr26204-112-ab300075'>ab300075</a>)
Predicted band size: 46 kDa
Observed band size: 50 kDa
false
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TRAF1 antibody [EPR26204-112] (BSA and Azide free) (AB300076)
This data was developed using ab300075, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat spleen tissue labelling TRAF1 with ab300075 at 1/100 (5.64 μg/ml) followed by a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) kit. Cytoplasmic staining on megakaryocytes in rat spleen (PMID : 11046039). The section was incubated with ab300075 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) kit.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (BOND™ Polymer Refine Detection) was used.
Heat mediated antigen retrieval 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-TRAF1 antibody [EPR26204-112] (BSA and Azide free) (AB300076)
This data was developed using ab300075, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse spleen tissue labelling TRAF1 with ab300075 at 1/100 (5.64 μg/ml) followed by a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) kit. Cytoplasmic staining on megakaryocytes in mouse spleen (PMID : 11046039). The section was incubated with ab300075 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 Leica DS9800 (BOND™ Polymer Refine Detection) kit.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins
- IHC
Supplier Data
Immunohistochemistry - Anti-TRAF1 antibody [EPR26204-112] (BSA and Azide free) (AB300076)
This data was developed using ab300075, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Mouse spleen tissue labelling TRAF1 with ab300075 at 1/100 (5.64 µg/ml) followed by a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) kit. Cytoplasmic staining on megakaryocytes in mouse spleen (PMID : 11046039). The section was incubated with ab300075 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 Leica DS9800 (BOND™ Polymer Refine Detection) kit. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TRAF1 antibody [EPR26204-112] (BSA and Azide free) (AB300076)
This data was developed using ab300075, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Rat spleen tissue labelling TRAF1 with ab300075 at 1/100 (5.64 µg/ml) followed by a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) kit. Cytoplasmic staining on megakaryocytes in rat spleen (PMID : 11046039). The section was incubated with ab300075 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) kit. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TRAF1 antibody [EPR26204-112] (BSA and Azide free) (AB300076)
This data was developed using ab300075, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Mouse thymus tissue labelling TRAF1 with ab300075 at 1/100 (5.64 µg/ml) followed by a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) kit. Cytoplasmic staining on mouse thymus medulla (PMID : 11046039). The section was incubated with ab300075 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 Leica DS9800 (BOND™ Polymer Refine Detection) kit. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-TRAF1 antibody [EPR26204-112] (BSA and Azide free) (AB300076)
This data was developed using ab300075, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse thymus tissue labelling TRAF1 with ab300075 at 1/100 (5.64 μg/ml) followed by a ready to use Leica DS9800 (BOND™ Polymer Refine Detection) kit. Cytoplasmic staining on mouse thymus medulla (PMID : 11046039). The section was incubated with ab300075 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 Leica DS9800 (BOND™ Polymer Refine Detection) kit.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 mins
- WB
Supplier Data
Western blot - Anti-TRAF1 antibody [EPR26204-112] (BSA and Azide free) (AB300076)
This data was developed using ab300075, the same antibody clone in a different buffer formulation.
5% NFDM/TBST was used as blocking and iluting buffer.
Exposure time :
Lane 1-2 : 92 seconds
Lane3 : 3 minutes
Left-hand blot (lanes 1 & 2) was developed using a high sensitivity ECL substrate.
Lane 3 : Lysates were freshly made and used in WB test immediately to minimize protein degradation.
The expression profile/molecular weight observed is consistent with that described in the literature (PMID : 25321474, 25996949).
All lanes:
Western blot - Anti-TRAF1 antibody [EPR26204-112] (<a href='/en-us/products/primary-antibodies/traf1-antibody-epr26204-112-ab300075'>ab300075</a>) at 1/1000 dilution
Lane 1:
Ramos (human Burkitt's lymphoma B lymphocyte) whole cell lysate at 20 µg
Lane 2:
Daudi (human Burkitt's lymphoma lymphoblast) whole cell lysate at 20 µg
Lane 3:
Daudi whole cell fresh 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
Predicted band size: 46 kDa
Observed band size: 50 kDa
false
- WB
Supplier Data
Western blot - Anti-TRAF1 antibody [EPR26204-112] (BSA and Azide free) (AB300076)
This data was developed using ab300075, the same antibody clone in a different buffer formulation. 5% NFDM/TBST was used as blocking and iluting buffer. Lysates were freshly made and used in WB test immediately to minimize protein degradation. The expression profile/molecular weight observed is consistent with that described in the literature (PMID : 25321474, 25996949). Negative control : HEK-293 (PMID : 12502848)
All lanes:
Western blot - Anti-TRAF1 antibody [EPR26204-112] (<a href='/en-us/products/primary-antibodies/traf1-antibody-epr26204-112-ab300075'>ab300075</a>) at 1/1000 dilution
Lane 1:
Raji (human Burkitt's lymphoma B lymphocyte) whole cell fresh lysate at 20 µg
Lane 2:
HEK-293 (human embryonic kidney epithelial cell) whole cell fresh 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
Predicted band size: 46 kDa
Observed band size: 50 kDa
false
Exposure time: 15s
- WB
Supplier Data
Western blot - Anti-TRAF1 antibody [EPR26204-112] (BSA and Azide free) (AB300076)
This data was developed using ab300075, the same antibody clone in a different buffer formulation.
5% NFDM/TBST was used as blocking and iluting buffer.
Lysates were freshly made and used in WB test immediately to minimize protein degradation.
The expression profile/molecular weight observed is consistent with that described in the literature (PMID : 25321474, 25996949).
Negative control : HEK-293 (PMID : 12502848)
All lanes:
Western blot - Anti-TRAF1 antibody [EPR26204-112] (<a href='/en-us/products/primary-antibodies/traf1-antibody-epr26204-112-ab300075'>ab300075</a>) at 1/1000 dilution
Lane 1:
Raji (human Burkitt's lymphoma B lymphocyte) whole cell fresh lysate at 20 µg
Lane 2:
HEK-293 (human embryonic kidney epithelial cell) whole cell fresh 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
Predicted band size: 46 kDa
Observed band size: 50 kDa
false
Exposure time: 15s
- WB
Supplier Data
Western blot - Anti-TRAF1 antibody [EPR26204-112] (BSA and Azide free) (AB300076)
This data was developed using ab300075, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
This blot was developed using a high sensitivity ECL substrate. The high-sensitivity ECL substrate used allows for the detection of proteins in the mid-femtogram range.
The expression profile/molecular weight observed is consistent with that described in the literature (PMID : 25321474, 25996949).
All lanes:
Western blot - Anti-TRAF1 antibody [EPR26204-112] (<a href='/en-us/products/primary-antibodies/traf1-antibody-epr26204-112-ab300075'>ab300075</a>) at 1/1000 dilution
Lane 1:
Human tonsil tissue lysate at 20 µg
Lane 2:
Human lymphoma 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
Predicted band size: 46 kDa
Observed band size: 50 kDa
true
Exposure time: 92s
- WB
Supplier Data
Western blot - Anti-TRAF1 antibody [EPR26204-112] (BSA and Azide free) (AB300076)
This data was developed using ab300075, the same antibody clone in a different buffer formulation.
5% NFDM/TBST was used as blocking and diluting buffer.
This blot was developed using a high sensitivity ECL substrate.
The expression profile/molecular weight observed is consistent with that described in the literature (PMID : 25321474, 25996949).
All lanes:
Western blot - Anti-TRAF1 antibody [EPR26204-112] (<a href='/en-us/products/primary-antibodies/traf1-antibody-epr26204-112-ab300075'>ab300075</a>) at 1/1000 dilution
Lane 1:
Human tonsil tissue lysate at 20 µg
Lane 2:
Human lymphoma 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
Predicted band size: 46 kDa
Observed band size: 50 kDa
false
Exposure time: 92s
- WB
Supplier Data
Western blot - Anti-TRAF1 antibody [EPR26204-112] (BSA and Azide free) (AB300076)
This data was developed using ab300075, the same antibody clone in a different buffer formulation. 5% NFDM/TBST was used as blocking and diluting buffer. Exposure time : Lane 1-2 : 92 seconds Lane3 : 3 minutes Left-hand blot (lanes 1 & 2) was developed using a high sensitivity ECL substrate. Lane 3 : Lysates were freshly made and used in WB test immediately to minimize protein degradation. The expression profile/molecular weight observed is consistent with that described in the literature (PMID : 25321474, 25996949).
All lanes:
Western blot - Anti-TRAF1 antibody [EPR26204-112] (<a href='/en-us/products/primary-antibodies/traf1-antibody-epr26204-112-ab300075'>ab300075</a>) at 1/1000 dilution
Lane 1:
Ramos (human Burkitt's lymphoma B lymphocyte) whole cell lysate, at 20 µg
Lane 2:
Daudi (human Burkitt's lymphoma lymphoblast) whole cell lysate at 20 µg
Lane 3:
Daudi whole cell fresh 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
Predicted band size: 46 kDa
Observed band size: 50 kDa
false
Related conjugates and formulations (1)
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Anti-TRAF1 antibody [EPR26204-112]
Reactivity data
Product details
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.
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.
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
TRAF1 plays a role in immune response regulation functioning as part of a larger TRAF protein complex that includes TRAF2 and TRAF3. This complex is significant for propagating signaling cascades important for immune system development and homeostasis. TRAF1 impacts the transcriptional activity that modulates inflammatory responses. It achieves this by interacting with other proteins to transmit signals from the cell surface to the nucleus subsequently affecting gene expression.
Pathways
TRAF1 is involved in the NF-κB and JNK signaling pathways which are important for immune cell activation and apoptosis regulation. In the NF-κB pathway TRAF1 works closely with TRAF2 facilitating the recruitment and activation of IKK (IκB kinase) which leads to the release and nuclear translocation of NF-κB. In the JNK pathway TRAF1 indirectly influences MAP kinase signaling cascades affecting cytokine production and cell death. These roles in signal transduction highlight TRAF1's function in maintaining immune cell function and integrity.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
iScience 26:107601 PubMed37664606
2023
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
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