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Astor Scientific  |  SKU: ASTP5971

Human TARDBP (Tar Dna-Binding Protein 43) - Recombinant Protein

Molecule: TARDBP
Species: Human
Expression System: E.coli
Tag: N-6His
Expression Range: 1-260aa
$429.99 $549.99
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SDS-PAGE analysis of Human TARDBP (Tar Dna-Binding Protein 43) - Recombinant Protein, showing >85% purity under 15% SDS-PAGE (Reduced)
Astor Scientific

Human TARDBP (Tar Dna-Binding Protein 43) - Recombinant Protein

$429.99 $549.99

Product Overview

Product Name Recombinant Human TARDBP Protein
Product Overview This recombinant human TARDBP protein includes amino acids 1-260aa of the target gene is expressed in E.coli.The protein is supplied in lyophilized form and formulated in phosphate buffered saline (pH7.4) containing 0.01% sarcosyl, 5% trehaloseprior to lyophilization.
Target Uniprot Id Q13148
Recommended Name TAR DNA-binding protein 43
Gene Name TARDBP
Synonyms TAR DNA binding protein, ALS10, TDP43
Species Human
Predicted Molecular Mass 33.6 kDa
Expression System E.coli
Expression Range 1-260aa
Tag N-6His
Purity >85%
Formulation Lyophilized
Buffer Phosphate buffered saline (pH7.4) containing 0.01% sarcosyl, 5%Trehalose
Storage Condition 1. Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. 2. Avoid repeated freeze-thaw cycles. 3. Store working aliquots at 4°C for up to one week. 4. In general, protein in liquid form is stable for up to 6 months at -20°C/-80°C. Protein in lyophilized powder form is stable for up to 12 months at -20°C/-80°C.
Reconstitution Instruction Briefly centrifuged the vial prior to opening to bring the contents to the bottom. Reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL. It is recommended to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20°C/-80°C. The default final concentration of glycerol is 50%.
Applications Positive Control; Immunogen; SDS-PAGE; WB
Research Area Microbiology, Transcription
Target 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. Regulates also 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. Participates also 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.
Subcellular Location Nucleus. Cytoplasm. Cytoplasm, Stress granule.
Associated Diseases Amyotrophic lateral sclerosis 10 (ALS10)
Tissue Specificity Ubiquitously expressed. In particular, expression is high in pancreas, placenta, lung, genital tract and spleen.

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  • 100ug
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