TAR DNA bindingseiwit 43 Antilichaam / TDP43 / TARDBP

It participates in stress-responsive RNA granule dynamics and controlled phase behavior, linking RNA sorting to protein quality control pathways. Its nuclear enrichment, regulated export, and post-translational modification states offer quantitative readouts for studies of RNA processing, trafficking, and cellular adaptation in defined model systems. The TAR DNA binding protein 43 antibody from NSJ Bioreagents enables specific detection of endogenous TDP-43 in applications such as western blot, immunofluorescence, immunohistochemistry, immunoprecipitation, and RNA-protein pulldown workflows. Researchers use the TAR DNA binding protein 43 antibody to measure total protein levels, assess nuclear-cytoplasmic distribution, and evaluate biochemical fractionation or stress-induced relocalization when paired with appropriate complementary reagents. With high specificity and reproducible performance, the TAR DNA binding protein 43 antibody supports rigorous analysis of RNA-binding protein networks and post-transcriptional regulation. TAR DNA binding protein 43 antibody

Western blot: 1:500-1:2000, Immunohistochemistry (FFPE) : 1:50-1:200, Immunofluorescence: 1:50-1:200

Q13148

Human, Mouse, Rat

A peptide sequence specific to TAR DNA binding protein 43 was used as the immunogen for the TAR DNA binding protein 43 antibody.

26T75

WB, IF, IHC-P

Affinity chromatography

Purified

This TAR DNA binding protein 43 antibody is available for research use only.

After reconstitution, the TAR DNA binding protein 43 Antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.

Antibody in PBS with 0.02% sodium azide, 50% glycerol and 0.4-0.5 mg/mL BSA

Optimal dilution of the TAR DNA binding protein 43 antibody should be determined by the researcher.

Nuclear, cytoplasmic

IHC staining of FFPE human glioma tissue with TAR DNA binding protein 43 antibody, HRP-secondary and DAB substrate. HIER: boil tissue sections in pH8 EDTA for 20 min and allow to cool before testing.