Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5'-Atp | HCID 5957 | — |
| Reactant | Ethylenediaminetetraacetic Acid | HCID 6049 | — |
| Reactant | X 100 | HCID 19153 | — |
| Reactant | Coenzyme A | HCID 87642 | — |
| Reactant | Leupeptin acid | HCID 189069 | — |
| Reactant | Sodium Lauryl Sulfate | HCID 3423265 | — |
| Solvent | 4-(2-Hydroxyethyl)-1-piperazineethanesulfonic acid | HCID 23831 | — |
| Solvent | Tromethamine hydrochloride | HCID 93573 | — |
| Product | Palmitic Acid | HCID 985 | — |
Reaction Steps
Soluble Shh was labeled with 3H-palmitic acid in a cell-free system using a modified version of a published procedure (24). A crude microsomal fraction from rat liver was prepared by subjecting a liver homogenate to sequential centrifugation at 3000×g for 10 min, 9000×g for 20 min, and 100,000×g for 30 min. The 100,000×g pellet was suspended in 10 mM HEPES pH 7.4, 10% sucrose and again centrifuged at 100,000×g for 20 min. The final pellet (derived from 10 g of liver) was suspended in 3 mL of 20 mM Tris-HCl pH 7.4, 150 mM NaCl, 1 mM EDTA, 10 μg/mL leupeptin, 0.15% Triton X-100, aliquoted, and stored at −70° C. Reactions containing 3 μg Shh, 1 μL of rat microsomes, 50 ng/mL Coenzyme A (Sigma), 0.3 mM ATP, 20 mM Tris-HCl pH 7.4, 150 mM NaCl, 1 mM EDTA, 10 μg/mL leupeptin, and 0.5 μCi-[9,10-3H]-palmitic acid (50 Ci/mmol; New England Nuclear) were performed at room temperature for 1 h. Reactions were stopped with reducing electrophoresis sample buffer, subjected to SDS-PAGE on a 10-20% gradient gel, and visualized by fluorography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06444793B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-ca440bf402f441fcbcfc7df96221cafd |
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| Source note | uspto-grants-2002_09 |
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