Anti-Trans-Golgi network integral membrane protein 1 抗体 [EPR24831-36] - BSA and Azide free
Anti-Trans-Golgi network integral membrane protein 1 antibody [EPR24831-36] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal Trans-Golgi network integral membrane protein 1 antibody. Carrier free. Suitable for ICC/IF, WB, IHC-P, Flow Cyt (Intra), IP and reacts with Mouse samples.
查看别名
Ttgn1, Tgoln1, Trans-Golgi network integral membrane protein 1, TGN38A
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Trans-Golgi network integral membrane protein 1 antibody [EPR24831-36] - BSA and Azide free (AB283702)
This data was developed using ab283678, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 100% methanol-fixed, 0.1% TritonX-100 permeabilized C2C12 cells labelling TGN38 with ab283678 at 1/50 (11.38 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2 ug/ml) dilution (Green). Confocal image showing co-locolization positive staining with Golgi marker in C2C12 cells is observed. ab169276 Anti-GM130 mouse polyclonal antibody - cis-Golgi Marker was used to counterstain tubulin at 1/200 5ug/ml dilution (Red). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/ml) dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Trans-Golgi network integral membrane protein 1 antibody [EPR24831-36] - BSA and Azide free (AB283702)
This data was developed using ab283678, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse kidney tissue labelling TGN38 with ab283678 at 1/2000 (0.285 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Granular cytoplasmic staining in mouse kidney. The section was incubated with ab283678 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 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-Trans-Golgi network integral membrane protein 1 antibody [EPR24831-36] - BSA and Azide free (AB283702)
This data was developed using ab283678, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse liver tissue labelling TGN38 with ab283678 at 1/2000 (0.285 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Granular cytoplasmic staining in mouse liver. The section was incubated with ab283678 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 with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-Trans-Golgi network integral membrane protein 1 antibody [EPR24831-36] - BSA and Azide free (AB283702)
This data was developed using ab283678, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized C2C12 (Mouse myoblasts myoblast) cells labelling TGN38 with ab283678 at 1/500 dilution (0.1ug) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat F(ab')2 Anti-Rabbit IgG (DyLight® 488, ab98507) at 1/500 dilution was used as the secondary antibody.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Trans-Golgi network integral membrane protein 1 antibody [EPR24831-36] - BSA and Azide free (AB283702)
This data was developed using ab283678, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labelling TGN38 with ab283678 at 1/2000 (0.285 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Granular cytoplasmic staining in mouse cerebrum. The section was incubated with ab283678 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 with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-Trans-Golgi network integral membrane protein 1 antibody [EPR24831-36] - BSA and Azide free (AB283702)
This data was developed using ab283678, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized NIH/3T3 (Mouse embryonic fibroblast) cells labelling TGN38 with ab283678 at 1/500 dilution (0.1ug) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat F(ab')2 Anti-Rabbit IgG (DyLight® 488, ab98507) at 1/500 dilution was used as the secondary antibody.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Trans-Golgi network integral membrane protein 1 antibody [EPR24831-36] - BSA and Azide free (AB283702)
This data was developed using ab283678, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 100% methanol-fixed, 0.1% TritonX-100 permeabilized NIH/3T3 cells labelling TGN38 with ab283678 at 1/50 (11.38 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2 ug/ml) dilution (Green). Confocal image showing co-locolization positive staining with Golgi marker in NIH/3T3 cells is observed. ab169276 Anti-GM130 mouse polyclonal antibody - cis-Golgi Marker was used to counterstain tubulin at 1/200 5ug/ml dilution (Red). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/ml) dilution.
- IP
Supplier Data
Immunoprecipitation - Anti-Trans-Golgi network integral membrane protein 1 antibody [EPR24831-36] - BSA and Azide free (AB283702)
This data was developed using ab283678, the same antibody clone in a different buffer formulation.
TGN38 was immunoprecipitated from 0.35 mg C2C12 (mouse myoblasts myoblast), whole cell lysate 10 ug with ab283678 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab283678 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : C2C12 (mouse myoblasts myoblast), whole cell lysate 10 ug
Lane 2 : ab283678 IP in C2C12 whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab283678 in C2C12 whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 49 seconds
This blot was developed using a higher sensitivity ECL substrate.
All lanes:
Immunoprecipitation - Anti-Trans-Golgi network integral membrane protein 1 antibody [EPR24831-36] (<a href='/products/primary-antibodies/trans-golgi-network-integral-membrane-protein-1-antibody-epr24831-36-ab283678'>ab283678</a>)
Predicted band size: 38 kDa
Observed band size: 75 kDa
false
- WB
Lab
Western blot - Anti-Trans-Golgi network integral membrane protein 1 antibody [EPR24831-36] - BSA and Azide free (AB283702)
This data was developed using ab283678, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Lane 1 of this blot was developed using a higher sensitivity ECL substrate.
The expression profiles/observed MW are consistent with what has been described in the literature (PMID : 12494998).
Exposure time : 3 minutes
All lanes:
Western blot - Anti-Trans-Golgi network integral membrane protein 1 antibody [EPR24831-36] (<a href='/products/primary-antibodies/trans-golgi-network-integral-membrane-protein-1-antibody-epr24831-36-ab283678'>ab283678</a>) at 1/1000 dilution
Lane 1:
NIH/3T3 (mouse embryonic fibroblast), whole cell lysate at 20 µg
Lane 2:
C2C12 (mouse myoblasts myoblast), whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 38 kDa
Observed band size: 85 kDa
false
- WB
Lab
Western blot - Anti-Trans-Golgi network integral membrane protein 1 antibody [EPR24831-36] - BSA and Azide free (AB283702)
This data was developed using ab283678, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST
This antibody has cross-reaction with mouse TGN38B.
The recombinant proteins TGN38B and TGN38 were made in-house.
The sample loaded onto lane 1 was purified TGN38B recombinant protein expressed from an E.coli expression system.
The sample loaded onto lanes 2 was purified TGN38 recombinant protein expressed from a mammalian - HEK-293 expression system.
Exposure time : 81 seconds
All lanes:
Western blot - Anti-Trans-Golgi network integral membrane protein 1 antibody [EPR24831-36] (<a href='/products/primary-antibodies/trans-golgi-network-integral-membrane-protein-1-antibody-epr24831-36-ab283678'>ab283678</a>) at 1/1000 dilution
Lane 1:
His-tagged mouse TGN38B recombinant protein at 0.01 µg
Lane 2:
LIF-tagged mouse TGN38 recombinant protein at 0.01 µg
Secondary
Lane 1:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Lane 2:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 38 kDa
Observed band size: 50 kDa,65-100 kDa
false
不同偶联物与剂型 (1)
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Anti-Trans-Golgi network integral membrane protein 1 antibody [EPR24831-36]
反应性数据
产品详情
ab283702 is the carrier-free version of ab283678.
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.
性能和储存信息
形式
纯化工艺
存储溶液
运输条件
推荐的短期储存条件
推荐的长期储存条件
补充信息
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The protein is involved in maintaining the structure and function of the trans-Golgi network. TGOLN2 works as part of a complex network that includes multiple integral membrane proteins which regulate vesicular trafficking. Its ability to bind with other proteins facilitates the sorting and packaging of secretory proteins which are then dispatched through vesicles. By efficiently working with the cellular machinery TGOLN2 contributes to the proper processing and delivery of proteins essential for cellular function.
Pathways
TGOLN2 significantly integrates in the protein trafficking and glycosylation pathways within cells. It cooperates closely with Kinesin and Dynein motor proteins to move vesicles along cytoskeletal tracks to their correct location. TGOLN2 also interacts with adaptin protein complexes which are important for the selection of cargo proteins destined for delivery to specific compartments. This positioning in pathways makes TGOLN2 an essential factor in ensuring the precise cellular localization of proteins.
产品实验方案
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靶点信息
Abcam 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