Human/Mouse/Rat TDP-43/TARDBP Antibody Summary
Met1-Thr103
Accession # Q13148
Applications
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Scientific Data
Detection of Human TDP-43/TARDBP by Western Blot. Western blot shows lysates of A431 human epithelial carcinoma cell line and NR8383 rat alveolar macrophage cell line. PVDF membrane was probed with 0.4 µg/mL of Mouse Anti-Human/Mouse/Rat TDP-43/TARDBP Monoclonal Antibody (Catalog # MAB7778) followed by HRP-conjugated Anti-Mouse IgG Secondary Antibody (HAF018). A specific band was detected for TDP-43/TARDBP at approximately 45 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 1.
Detection of Human and Mouse TDP-43/TARDBP by Western Blot. Western blot shows lysates of HeLa human cervical epithelial carcinoma cell line and RAW 264.7 mouse monocyte/macrophage cell line. PVDF membrane was probed with 1 µg/mL of Mouse Anti-Human TDP-43/TARDBP Monoclonal Antibody (Catalog # MAB7778) followed by HRP-conjugated Anti-Mouse IgG Secondary Antibody (HAF018). A specific band was detected for TDP-43/TARDBP at approximately 43 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 3.
TDP-43/TARDBP in A431 Human Cell Line. TDP-43/TARDBP was detected in immersion fixed A431 human epithelial carcinoma cell line using Mouse Anti-Human/Mouse/Rat TDP-43/TARDBP Monoclonal Antibody (Catalog # MAB7778) at 1 µg/mL for 3 hours at room temperature. Cells were stained using the NorthernLights™ 557-conjugated Anti-Sheep IgG Secondary Antibody (red; NL010) and counterstained with DAPI (blue). Specific staining was localized to nuclei. View our protocol for Fluorescent ICC Staining of Cells on Coverslips.
TDP-43/TARDBP in Human Brain. TDP-43/TARDBP was detected in immersion fixed paraffin-embedded sections of human brain (hippocampus) using Mouse Anti-Human/Mouse/Rat TDP-43/TARDBP Monoclonal Antibody (Catalog # MAB7778) at 1.7 µg/mL overnight at 4 °C. Tissue was stained using the Anti-Mouse HRP-DAB Cell & Tissue Staining Kit (brown; CTS002) and counterstained with hematoxylin (blue). Specific staining was localized to nuclei. View our protocol for Chromogenic IHC Staining of Paraffin-embedded Tissue Sections.
Detection of Human and Rat TDP-43/TARDBP by Simple WesternTM. Simple Western lane view shows lysates of A431 human epithelial carcinoma cell line and NR8383 rat alveolar macrophage cell line, loaded at 0.2 mg/mL. A specific band was detected for TDP-43/TARDBP at approximately 54 kDa (as indicated) using 5 µg/mL of Mouse Anti-Human TDP-43/TARDBP Monoclonal Antibody (Catalog # MAB7778). This experiment was conducted under reducing conditions and using the 12-230 kDa separation system. Non-specific interaction with the 230 kDa Simple Western standard may be seen with this antibody.
Detection of TDP-43/TARDBP by Immunoprecipitation. Immunoprecipitation was performed on cell lysate of HAP1 human near-haploid cell line using 2.0 μg of Mouse Anti-Human TDP-43 Monoclonal Antibody (Catalog # MAB7778) pre-coupled to protein G or protein A beads. Immunoprecipitated TDP-43/TARDBP was detected with a Rabbit Anti-TDP-43 antibody. The Ponceau stained transfers of each blot are shown. SM=10% starting material; UB=10% unbound fraction; IP=immunoprecipitated. Image, protocol, and testing courtesy of YCharOS Inc. (ycharos.com).
Reconstitution Calculator
Preparation and Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Background: TDP-43/TARDBP
TDP-43 (TAR DNA binding protein of 43 kDa; gene name TARDBP) is a 414 amino acid (aa) nuclear RNA/DNA binding phosphoprotein that regulates transcription and splicing. TDP-43 is aberrantly expressed in most forms of amylotrophic lateral sclerosis and frontotemporal lobar degeneration. In these cases it is absent from the nucleus and accumulates, along with a truncated 20-28 kDa form, in ubiquitin-containing inclusion bodies. TDP-43 can also influence CFTR exon 9 skipping in cystic fibrosis. Within aa 1-103, human and mouse TDP-43 share 100% aa sequence identity, and 99% aa identity with rat TDP-43.
Product Datasheets
Citations for Human/Mouse/Rat TDP-43/TARDBP Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
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Citations: Showing 1 - 6
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Loss of TMEM106B and PGRN leads to severe lysosomal abnormalities and neurodegeneration in mice
Authors: Feng T, Mai S, Roscoe JM et al.
EMBO Rep.
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TMEM106B deficiency impairs cerebellar myelination and synaptic integrity with Purkinje cell loss
Authors: T Feng, L Luan, II Katz, M Ullah, VM Van Deerli, JQ Trojanowsk, EB Lee, F Hu
Acta neuropathologica communications, 2022-03-14;10(1):33.
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The identification of high-performing antibodies for TDP-43 for use in Western Blot, immunoprecipitation and immunofluorescence
Authors: Worrall, D;Ayoubi, R;Fotouhi, M;Southern, K;McPherson, PS;Laflamme, C;NeuroSGC/YCharOS/EDDU collaborative group, ;ABIF Consortium, ;
F1000Research
Species: Human
Sample Types: Cell Lysates
Applications: Western Blot -
Epithelial-derived factors induce muscularis mucosa of human induced pluripotent stem cell-derived gastric organoids
Authors: K Uehara, M Koyanagi-A, T Koide, T Itoh, T Aoi
Stem Cell Reports, 2022-03-03;0(0):.
Species: Mouse
Sample Types: Tissue Lysates
Applications: Western Blot -
Long non-coding RNA NEAT1_1 ameliorates TDP-43 toxicity in in vivo models of TDP-43 proteinopathy
Authors: Koji Matsukawa, Michail S. Kukharsky, Sei-Kyoung Park, Sangeun Park, Naruaki Watanabe, Takeshi Iwatsubo et al.
RNA Biology
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Generation and analysis of innovative genomically humanized knockin SOD1, TARDBP (TDP-43), and FUS mouse models
Authors: Devoy A, Price G, De Giorgio F Et al.
iScience
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