Immunodetection Reagents & Substrates

casein kinase I substrate (RRKDLHDDEEDEAMSITA) is a synthetic peptide substrate for casein kinase I. There is negligible phosphorylation rate of this substrate by casein kinase II.

CREBtide is a synthetic substrate for PKA and PKC. The sequence is based on the phosphorylation sequence in δ-CREB (cAMP response element binding protein).

DCB is an allosteric ligand for the metabotropic glutamate receptor mGluR-5 and displays neutral modulation. DCB does not affect agonist-stimulated mGluR-5 responses, but blocks regulation of the receptor by other allosteric modulators such as DFB

DCB is an allosteric ligand for the metabotropic glutamate receptor mGluR-5 and displays neutral modulation. DCB does not affect agonist-stimulated mGluR-5 responses, but blocks regulation of the receptor by other allosteric modulators such as DFB

Decanoyl-p-nitroanilide is a synthetic fatty acid amide utilized as a probe for activity of FAAH (fatty acid amide hydrolase), the enzyme primarily responsible for degradation of the endocannabinoid Anandamide . FAAH accepts Decanoyl-p-nitroanilide

Decanoyl-p-nitroanilide is a synthetic fatty acid amide utilized as a probe for activity of FAAH (fatty acid amide hydrolase), the enzyme primarily responsible for degradation of the endocannabinoid Anandamide . FAAH accepts Decanoyl-p-nitroanilide

Binds to GABAAreceptor Cl-channel allosteric modulator of benzodiazepine site

Binds to GABAAreceptor Cl-channel allosteric modulator of benzodiazepine site

Binds to GABAAreceptor Cl-channel allosteric modulator of benzodiazepine site

Binds to GABAAreceptor Cl-channel allosteric modulator of benzodiazepine site

DPPE Fumarate has high affinity for the anti-estrogen binding site. Inhibits histamine binding at the intracellular histamine (Hlc) site. DPPE Fumarate does not bind to the estrogen receptor.

DPPE Fumarate has high affinity for the anti-estrogen binding site. Inhibits histamine binding at the intracellular histamine (Hlc) site. DPPE Fumarate does not bind to the estrogen receptor.