Anti-TAR DNA-binding protein 43 antibody (Full-Length) [3H8] (STJA0040756)

SPECIFICATIONS
ClonalityMonoclonal
HostMouse
ConjugationUnconjugated
IsotypeIgG
ImmunogenThis antibody was raised against recombinant full length human his-tagged TDP43 which was expressed in E. coli and purified by nickel affinity.
STJA0040756-100
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General Information

Short DescriptionMouse monoclonal anti-TAR DNA-binding protein 43 (Full-Length) for use in ICC, IHC-F and WB in Human, Mouse, Other Mammals and Rat samples. Datasheet included with dilution recommendations, and related reagents.
ApplicationsICC/IHC-F/WB
HostMouse
ReactivityHuman/Mouse/Other Mammals/Rat
NoteSTRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.

Product Properties

ClonalityMonoclonal
Clone ID3H8
IsotypeIgG
ConjugationUnconjugated
PurificationIgG
Dilution RangeWB 1:1000-1:5000
IHC 1:1000-1:5000
ICC 1:500-1:1000
FormulationLyophilized from PBS buffer pH 7.2-7.6 with 0.1% trehalose, and sodium azide
Storage InstructionSpin vial briefly before opening. Reconstitute with 100 ยตL sterile-filtered, ultrapure water to achieve a 1 mg/mL concentration. Centrifuge to remove any insoluble material. After reconstitution of lyophilized antibody, aliquot and store at-20ยฐC for

Target Information

Gene SymbolTARDBP
Gene ID23435
Uniprot IDTADBP_HUMAN
ImmunogenThis antibody was raised against recombinant full length human his-tagged TDP43 which was expressed in E. coli and purified by nickel affinity.
Immunogen RegionFull-Length
Immunogen SequenceHuman
SpecificityThe specificity of this antibody has been confirmed by WB. This antibody detects ~43 kDa TDP43 protein on crude extract of mouse brain nuclear fraction. Human and Rodent. Predicted to react with other mammalian tissue.

Additional Info

Tissue Specificity Ubiquitously expressed. In particular, expression is high in pancreas, placenta, lung, genital tract and spleen.
Post Translational Modifications Hyperphosphorylated in hippocampus, neocortex, and spinal cord from individuals affected with ALS and FTLDU. Phosphorylated upon cellular stress. Ubiquitinated in hippocampus, neocortex, and spinal cord from individuals affected with ALS and FTLDU. Cleaved to generate C-terminal fragments in hippocampus, neocortex, and spinal cord from individuals affected with ALS and FTLDU.
Function RNA-binding protein that is involved in various steps of RNA biogenesis and processing. Preferentially binds, via its two RNA recognition motifs RRM1 and RRM2, to GU-repeats on RNA molecules predominantly localized within long introns and in the 3'UTR of mRNAs. In turn, regulates the splicing of many non-coding and protein-coding RNAs including proteins involved in neuronal survival, as well as mRNAs that encode proteins relevant for neurodegenerative diseases. Plays a role in maintaining mitochondrial homeostasis by regulating the processing of mitochondrial transcripts. Also regulates mRNA stability by recruiting CNOT7/CAF1 deadenylase on mRNA 3'UTR leading to poly(A) tail deadenylation and thus shortening. In response to oxidative insult, associates with stalled ribosomes localized to stress granules (SGs) and contributes to cell survival. Also participates in the normal skeletal muscle formation and regeneration, forming cytoplasmic myo-granules and binding mRNAs that encode sarcomeric proteins. Plays a role in the maintenance of the circadian clock periodicity via stabilization of the CRY1 and CRY2 proteins in a FBXL3-dependent manner. Negatively regulates the expression of CDK6. Regulates the expression of HDAC6, ATG7 and VCP in a PPIA/CYPA-dependent manner.
Protein Name Tar Dna-Binding Protein 43
Tdp-43
Database Links
Cellular Localisation Nucleus
Cytoplasm
Stress Granule
Mitochondrion
Continuously Travels In And Out Of The Nucleus
Localizes To Stress Granules In Response To Oxidative Stress
A Small Subset Localizes In Mitochondria
Alternative Antibody Names Anti-Tar Dna-Binding Protein 43 antibody
Anti-Tdp-43 antibody
Anti-TARDBP antibody
Anti-TDP43 antibody

Information sourced from Uniprot.org

Citations

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