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Shank1

Manufactured by Synaptic Systems

Shank1 is a component used in research applications involving the study of neurological structures and processes. It serves as a specialized tool for precisely manipulating and positioning samples during microscopic analysis. The core function of Shank1 is to enable controlled and accurate positioning of specimens for detailed observation and investigation.

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2 protocols using shank1

1

Protein analysis of synaptic fractions

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PSD and synaptosomal fractions of the striatum, cortex, and cerebellum were prepared as previously described21 (link). Purified fractions were separated on SDS-PAGE and quantified using Odyssey Licor. β-Actin and Tubulin were used as loading controls. Specific primary antibody for SAPAP3 was prepared as previously described21 (link). Commercial antibodies used include SHANK3 (Santa Cruz SC-30193), GluR1 (Millipore MAB2263), GluR2 (Neuromab 75-002), NR1 (BD Biosciences 556308), NR2A (Millipore 07-632), NR2B (Millipore 05-920), Homer1 (Chemicon AB5877, Synaptic Systems 160022), Homer3 (Synaptic Systems 160303), mGLUR5 (Abcam ab76316), CaMKIIa (Millipore 05-532), Shank1 (Synaptic Systems 162002), Shank2 (Cell Signaling 12218S), B-Actin (Sigma A5441), and Tubulin (Sigma T5168). Statistical analysis was done using two-tailed Students’ t-tests.
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2

Protein analysis of synaptic fractions

Check if the same lab product or an alternative is used in the 5 most similar protocols
PSD and synaptosomal fractions of the striatum, cortex, and cerebellum were prepared as previously described21 (link). Purified fractions were separated on SDS-PAGE and quantified using Odyssey Licor. β-Actin and Tubulin were used as loading controls. Specific primary antibody for SAPAP3 was prepared as previously described21 (link). Commercial antibodies used include SHANK3 (Santa Cruz SC-30193), GluR1 (Millipore MAB2263), GluR2 (Neuromab 75-002), NR1 (BD Biosciences 556308), NR2A (Millipore 07-632), NR2B (Millipore 05-920), Homer1 (Chemicon AB5877, Synaptic Systems 160022), Homer3 (Synaptic Systems 160303), mGLUR5 (Abcam ab76316), CaMKIIa (Millipore 05-532), Shank1 (Synaptic Systems 162002), Shank2 (Cell Signaling 12218S), B-Actin (Sigma A5441), and Tubulin (Sigma T5168). Statistical analysis was done using two-tailed Students’ t-tests.
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