You Searched For: Pifithrin-\\\\u03B1+(cyclic)+hydrobromide

Catalog Number: (76743-754)

Supplier: ANTIBODIES.COM LLC

Description: Rat CD38 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the <i>in vitro</i> quantitative determination of rat CD38 in serum, plasma, tissue homogenates, and other biological fluids.

Catalog Number: (CAJTU497-9)

Supplier: AVANTOR PERFORMANCE MATERIAL LLC

Description: 1,2-Propanediol cyclic carbonate. CAS RN 108-32-7. Formula Weight: 102.09. Density: 1.20kg/L. Practical Grade. Subject to postal/shipping restrictions. 4L.

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Supplier: Bachem Americas

Description: Compstatin, ICVVQDWGHHRCT, is a 13-residue cyclic peptide that inhibits complement activation by binding to complement component C3.

Catalog Number: (10075-406)

Supplier: Prosci

Description: Polyclonal, Host: Rabbit; Species Reactivity: Mouse, Rat; Endogenous rabbit 2,3-cyclic nucleotide-3-phospho-diesterase; Tested Applications: WB

Catalog Number: (89160-360)

Supplier: Enzo Life Sciences

Supplier: Bachem Americas

Description: The cyclic MSH analog HS024 showed about 20-fold selectivity and very high affinity (Ki = 0.29 nM) for the melanocortin-4 (MC4) receptor and also increased the food intake, indicating that blockade of the MC4 receptor is a highly effective way to increase feeding.

Supplier: Thermo Scientific Chemicals

Description: Catalyzes the hydrolysis of N-terminal peptide bonds

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Catalog Number: (10331-868)

Supplier: Bioss

Description: Plays a role in signal transduction by regulating the intracellular concentration of cyclic nucleotides. This phosphodiesterase catalyzes the specific hydrolysis of cGMP to 5'-GMP (PubMed:9714779, PubMed:15489334). Specifically regulates nitric-oxide-generated cGMP (PubMed:15489334).

Catalog Number: (76085-278)

Supplier: Bioss

Description: Cyclic guanosine monophosphate (cGMP) serves as a second messenger in a manner similar to that observed with cAMP. Peptide hormones, such as the natriuretic factors, activate receptors that are associated with membrane-bound guanylate cyclase (GC). Receptor activation of GC leads to the conversion of GTP to cGMP. Nitric oxide (NO) also stimulates cGMP production by activating soluble GC, perhaps by binding to the heme moiety of the enzyme. Similar to cAMP, cGMP mediates most of its intracellular effects through the activation of specific cGMP dependent protein kinases (PKG).

Catalog Number: (76085-276)

Supplier: Bioss

Description: Cyclic guanosine monophosphate (cGMP) serves as a second messenger in a manner similar to that observed with cAMP. Peptide hormones, such as the natriuretic factors, activate receptors that are associated with membrane-bound guanylate cyclase (GC). Receptor activation of GC leads to the conversion of GTP to cGMP. Nitric oxide (NO) also stimulates cGMP production by activating soluble GC, perhaps by binding to the heme moiety of the enzyme. Similar to cAMP, cGMP mediates most of its intracellular effects through the activation of specific cGMP dependent protein kinases (PKG).

Catalog Number: (76120-942)

Supplier: Bioss

Description: Hyperpolarization-activated, cyclic nucleotide-binding channels (HCN) are voltage-gated cation channels that are activated by direct binding of intracellular cyclic nucleotides. The HCN family consists of four members (HCN1-4), each with a core transmembrane segment domain and a C-terminal 120 amino-acid cyclic nucleotide-binding domain motif. HCN channels are expressed in the brain, heart, thalamus and testis. The pacemaker properties of HCN channels contribute to spontaneous rhythmic activity in the brain and heart. HCN3 contains a segment characterized by a series of positively charged amino acids at every third position. This region designated S4 is likely to be the voltage sensor of the protein. In the brain, HCN3 and HCN4 exhibit subcortical distribution mainly concentrated in the hypothalamus and thalamus, respectively.

Catalog Number: (76101-618)

Supplier: Bioss

Description: Odorant signal transduction is probably mediated by a G-protein coupled cascade using cAMP as second messenger. The olfactory channel can be shown to be activated by cyclic nucleotides which leads to a depolarization of olfactory sensory neurons.

Catalog Number: (76120-944)

Supplier: Bioss

Description: Hyperpolarization-activated, cyclic nucleotide-binding channels (HCN) are voltage-gated cation channels that are activated by direct binding of intracellular cyclic nucleotides. The HCN family consists of four members (HCN1-4), each with a core transmembrane segment domain and a C-terminal 120 amino-acid cyclic nucleotide-binding domain motif. HCN channels are expressed in the brain, heart, thalamus and testis. The pacemaker properties of HCN channels contribute to spontaneous rhythmic activity in the brain and heart. HCN3 contains a segment characterized by a series of positively charged amino acids at every third position. This region designated S4 is likely to be the voltage sensor of the protein. In the brain, HCN3 and HCN4 exhibit subcortical distribution mainly concentrated in the hypothalamus and thalamus, respectively.

Catalog Number: (76101-620)

Supplier: Bioss

Description: Odorant signal transduction is probably mediated by a G-protein coupled cascade using cAMP as second messenger. The olfactory channel can be shown to be activated by cyclic nucleotides which leads to a depolarization of olfactory sensory neurons.

Supplier: Tonbo Biosciences

Description: The HIT2 antibody is specific for human CD38, a 45 kD type II transmembrane glycoprotein expressed on thymocytes, activated T and B cells, and monocytes as well as other non-hematopoietic cells. CD38 is an ectoenzyme that functions to catalyze the synthesis and hydrolysis of cyclic ADP-ribose and is involved in cell signaling, regulating cell adhesion, and activation. Additionally, CD38 has been shown to be a prognostic marker for some leukemias and other diseases.

Catalog Number: (H-2672.0001BA)

Supplier: Bachem Americas

Description: CRGDFPASSC is a cyclic RGD-containing decapeptide which binds to the fibrinogen receptor on the platelet surface. This analog with Phe substituted for Ser at position 5 was found to be 3 times more active (IC₅₀ = 2.5 µM) as a platelet aggregation inhibitor than CRGDSPASSC.