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Astor Scientific  |  SKU: ASTP4901

Human NRTN (Neurturin) - Recombinant Protein

Molecule: NRTN
Species: Human
Expression System: E.coli
Expression Range: 96-197aa
$429.99 $549.99
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SDS-PAGE analysis of Human NRTN (Neurturin) - Recombinant Protein, showing >95% purity under 15% SDS-PAGE (Reduced)
Astor Scientific

Human NRTN (Neurturin) - Recombinant Protein

$429.99 $549.99

Product Overview

Product Name Recombinant Human Neurturin (NRTN) Protein
Product Overview This recombinant human Neurturin (NRTN) protein includes amino acids 96-197aa 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 Q99748
Recommended Name Neurturin
Gene Name NRTN
Synonyms Neurturin; NRTN
Species Human
Predicted Molecular Mass 11.8 kDa
Expression System E.coli
Expression Range 96-197aa
Purity >95%
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
Target Function Supports the survival of sympathetic neurons in culture. May regulate the development and maintenance of the CNS. Might control the size of non-neuronal cell population such as haemopoietic cells.
Subcellular Location Secreted.
Protein Family TGF-beta family, GDNF subfamily
Associated Diseases Genetic variations in NRTN may contribute to Hirschsprung disease, in association with mutations of RET gene, and possibly mutations in other loci. Hirschsprung disease is a disorder of neural crest development is characterized by the absence of intramural ganglion cells in the hindgut, often resulting in intestinal obstruction.

Size

  • 100ug
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