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enQuireBio™ Recombinant Rat Leptin tA Protein
A cDNA sequence encoding the Leptin tA was constructed and used to recombinantly synthesize the protein.
£99.15 - £155.00
Specifications
Name | Leptin tA Protein |
---|---|
Regulatory Status | Research Use Only |
Endotoxin Concentration | < 1.0 EU per ug protein as determined by the LAL method. |
Biological Activity | Leptin Antagonist Triple Mutant Rat Recombinant half-life in circulation after SC injection was over 20 hours. Leptin Antagonist Triple Mutant Rat Recombinant is capable of inhibiting leptin-induced proliferation of BAF/3 cells stably transfected with the long form of human leptin receptor. Leptin Antagonist Triple Mutant Rat Recombinant in vitro activity is 5-6 fold lower than the non-pegylated antagonist, though in vivo it has profound weight gain effect (as compared to the non-pegylated antagonist), resulting mainly from increased food intake. |
Product Type | Recombinant Protein |
Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
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Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
15965098
|
enQuireBio™
QP10765-5ug |
5 μg |
£99.15
5µg |
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15955098
|
enQuireBio™
QP10765-20ug |
20 μg |
£155.00
20µg |
Please sign in to purchase this item. Need a web account? Register with us today! | |||||
Specifications
Leptin tA Protein | |
< 1.0 EU per ug protein as determined by the LAL method. | |
Recombinant Protein | |
E. coli | |
The Rat Leptin triple antagonist was lyophilized from a concentrated (0.65 mg/ml) solution with 0.003mM NaHCO3. |
Research Use Only | |
Leptin Antagonist Triple Mutant Rat Recombinant half-life in circulation after SC injection was over 20 hours. Leptin Antagonist Triple Mutant Rat Recombinant is capable of inhibiting leptin-induced proliferation of BAF/3 cells stably transfected with the long form of human leptin receptor. Leptin Antagonist Triple Mutant Rat Recombinant in vitro activity is 5-6 fold lower than the non-pegylated antagonist, though in vivo it has profound weight gain effect (as compared to the non-pegylated antagonist), resulting mainly from increased food intake. | |
Rat | |
Untagged | |
Greater than 99.0% as determined by:(a) Gel filtration analysis. (b) Analysis by SDS-PAGE. |