Esta buscando: ENZO LIFE SCIENCES

Numero del catalogo: (ENZOENZABS3000100)

Proveedor: ENZO LIFE SCIENCES

Descripción: Recommended Applications: Flow Cytometry, IF, IHC, WB

Species reactivity: Human, Rat, Monkey, Dog

UOM: 1 * 100 µl

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Numero del catalogo: (ENZOENZABS3020001)

Proveedor: ENZO LIFE SCIENCES

Descripción: Digoxigenin (DIG) is a steroid found exclusively in the flowers and leaves of the plants Digitalis purpurea and Digitalis lanata. DIG is the steroid component of digoxin, a cardiac glycoside, and can be conjugated onto a variety of biomolecules (proteins, nucleic acids) to be detected in further assays (e.g. ELISA). These antibodies can be labeled with dyes, enzymes or fluorescence, directly or secondarily, for visualization and detection.
DIG has an advantage over biotin due to the fact that biotin is an endogenous molecule of living cells and plays a key role in many reactions, which can sometimes lead to false positive results. Because the blossoms and leaves of Digitalis plants are the only natural sources of digoxigenin, binding of the anti-digoxigenin antibody in other biological material is not a consideration.

UOM: 1 * 1 mg

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Numero del catalogo: (ENZOENZABS2750100)

Proveedor: ENZO LIFE SCIENCES

Descripción: Recommended Applications: ELISA, WB

Species reactivity: Human

UOM: 1 * 100 µG

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Numero del catalogo: (ENZOENZABS2990100)

Proveedor: ENZO LIFE SCIENCES

Descripción: Recommended Applications: ELISA, IF, IHC (PS), WB

Species reactivity: Human, Mouse

UOM: 1 * 100 µG

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Numero del catalogo: (ENZOENZABS2590100)

Proveedor: ENZO LIFE SCIENCES

Descripción: Recommended Applications: IHC (PS), WB

UOM: 1 * 100 µG

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Numero del catalogo: (ENZOENZABS2940100)

Proveedor: ENZO LIFE SCIENCES

Descripción: Recommended Applications: IF, IP, WB

Species reactivity:

UOM: 1 * 100 µG

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Numero del catalogo: (ENZOENZABS2880050)

Proveedor: ENZO LIFE SCIENCES

Descripción: Recommended Applications: ELISA, ICC, IF, IP, WB

Species reactivity: Species independent

UOM: 1 * 50 µl

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Numero del catalogo: (ENZOADI905900100)

Proveedor: ENZO LIFE SCIENCES

Descripción: The cannabinoid receptors CB1 (expressed primarily throughout the central nervous system) and CB2 (expressed in peripheral tissues) are members of the seven-transmembrane domain-containing family of G-protein coupled receptors (GPCRs), and are named for their signaling function in response to cannabinoid drugs such as delta-9-tetrahydrocannabinol (delta-9-THC). Significant evidence suggests that additional cannabinoid receptors may contribute to the many behavioral, vascular, and immunological effects of agonists such as THC and endogenous cannabinoids. Evidence suggests GPR55 may act as a cannabinoid receptor, although its definition as a bona fide "CB3" receptor remains controversial. GPR55 is highly expressed in large-diameter dorsal root ganglion (DRG) neurons, and its activation by cannabinoid compounds (THC, JWH015, and anandamide) has been shown to release calcium from IP3-sensitive ER stores. These findings are opposed by evidence that suggests GPR55 is an intrinsic receptor for lysophosphatidylinositol (LPI).

UOM: 1 * 100 µG

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Numero del catalogo: (ENZOADI905800100)

Proveedor: ENZO LIFE SCIENCES

Descripción: The conversion of arachidonic acid to prostaglandin H2 (PGH2) by cyclooxygenase (COX) enzymes is the first step in the synthesis of prostanoids. Prostaglandin D2 (PGD2) is synthesized from PGH2 by the action of PGD synthase, and its actions in vasodilation and platelet activation are mediated via activation of two identified G-protein coupled receptors (GPCRs): DP1 and DP2 (formerly CRTH2). Both DP1 and DP2 receptors are coupled to Gs alpha subunits, resulting in increased adenylyl cyclase activity and cAMP production upon agonist binding. DP1 receptor is expressed moderately in the ileum and weakly in the lung, stomach, and uterus of mice, and weakly in the small intestine of humans. In rodents, expression of PGD synthase and the DP1 receptor is seen in the leptomeninges, where it is believed they play a role in the induction of sleep. The DP1 receptor may also oppose DP2-mediated activation of basophils, eosinophils, and Th2 cells.

UOM: 1 * 100 µG

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Numero del catalogo: (ENZOADI905744100)

Proveedor: ENZO LIFE SCIENCES

Descripción: The opioid receptors δ, κ, and μ are members of the seven-transmembrane domain-containing receptor family of G-protein coupled receptors. δ- and μ-receptors serve as functional receptors for endogenous enkephalin and β-endorphin peptide ligands, respectively. δ-opioid receptors are highly expressed in the olfactory bulb, neocortex, caudate putamen and nucleus accumbens, with peripheral expression in the gastro-intestinal tract and vas deferens. δ-receptors inhibit neurotransmitter release resulting in a variety of biological effects including analgesia, motor integration, gastro-intestinal motility, olfaction, respiration, and memory. Neural μ-receptor expression is prominent in the caudate putamen, neocortex, thalamus, nucleus accumbens, hippocampus, and amygdala, as well as in peripheral nervous tissues in the gut. Named for its pharmacological mediation of analgesia by morphine, the μ receptor typically functions as a depressant in physiological processes including respiration, cardiovascular function, gastrointestinal motility, and thermoregulation.

UOM: 1 * 100 µG

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Numero del catalogo: (ENZOADI905750100)

Proveedor: ENZO LIFE SCIENCES

Descripción: Arginine vasopressin (AVP) is a nonapeptide hormone produced in magnocellular neurons of the hypothalamus, which functions as an antidiuretic in the kidney and systemically as a regulator of vasoconstriction, blood volume, and blood pressure. AVP acts by binding to a set of specific seven transmembrane domain-containing G-protein coupled receptors (GPCR) classified into three groups: V1a (V1), V1b (V3), and V2. V1b receptors stimulate adrenocorticotropic hormone (ACTH) release in the anterior pituitary, but may also participate in corticotropin-releasing hormone (CRH) release by the hypothalamus. The V1b receptor signals through coupling of Gq/11 alpha subunits, activating phospholipase C and release of intracellular Ca2+ via phosphoinositide second messengers. V1b receptor overexpression is a common marker for ACTH-secreting corticotropic adenomas. V2 receptors in the collecting ducts of the kidneys stimulate adenylyl cyclase activity, regulating the reabsorption of water via aquaporin channels.

UOM: 1 * 100 µG

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Numero del catalogo: (ENZOADI905721100)

Proveedor: ENZO LIFE SCIENCES

Descripción: Beclin-1 is a coiled-coil Bcl-2-interacting protein that functions in autophagy, the process of bulk degradation of cellular proteins. Beclin-1 is homologous to the yeast autophagy gene apg6, and is expressed at reduced levels in human breast carcinoma, suggesting that defects in autophagy proteins may contribute to the development or progression of tumors. Bcl-2 can inhibit Beclin-1-dependent autophagy in yeast and mammalian cells, suggesting that Bcl-2 functions as both an anti-autophagic and anti-apoptotic protein.

UOM: 1 * 100 µG

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Numero del catalogo: (ENZOADI905743100)

Proveedor: ENZO LIFE SCIENCES

Descripción: The actions of the octapeptide circulatory hormone angiotensin II are mediated by type one (AT1) and type two (AT2) angiotensin II receptors, members of the seven-transmembrane domain-containing GPCR family. AT1 expression is greatest in vascular smooth muscle, liver, kidney, adrenal cortex, brain, and lung, and is primarily responsible for the physiological effects of angiotensin II in cardiovascular homeostasis. The AT2 receptor displays approximately 30% identity to the AT1 receptor, and is highly expressed during embryonic development. AT2 expression in adult tissue is limited to the adrenal medulla, brain, and reproductive tissues, but is upregulated in injured tissue following myocardial infarction, vascular injury, and wound healing.

UOM: 1 * 100 µG

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Numero del catalogo: (ENZOADI905741100)

Proveedor: ENZO LIFE SCIENCES

Descripción: Serotonin (5-hydroxytryptamine, 5-HT) is a monoamine found in the central nervous system, gastrointestinal tract, and blood with broad physiological functions as a neurotransmitter, in gastric motility, hemostasis, and cardiovascular integrity. Seven subclasses (5-HT 1-7) of serotonin receptors have been identified, a majority of which are members of the seven transmembrane domain-containing G-protein coupled receptor (GPCR) family, and are the target of several anti-depressant drugs. The 5-HT1 subclass consists of five highly homologous receptors that couple via G(i/o) alpha subunits to inhibit adenylyl cyclase activity. The 5-HT1A receptor gene is 99% homologous between human and mouse, and is expressed from an intronless gene with a predicted length of 421 amino acids. 5-HT1A receptor activation is generally inhibitory to cAMP production, but may also stimulate type II adenylyl cyclase activity in a cell-specific manner via release of G(beta/gamma) subunits when coupled to G(i2). 5-HT1A expression in mammals is strongest in CNS limbic pathways that control emotion, including tissue of the hippocampus, dorsal raphé, and septum.

UOM: 1 * 100 µG

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Numero del catalogo: (ENZOADI905791100)

Proveedor: ENZO LIFE SCIENCES

Descripción: Endothelins are vasoactive peptides that exist in three forms (ET-1, ET-2, and ET-3), and function in the maintenance of vascular tone via two identified seven transmembrane-spanning domain-containing G protein-coupled receptors (GPCR), endothelin A (ETA) and endothelin B (ETB). The human ETA receptor is primarily expressed in vascular smooth muscle cells, including those of the heart (also in myocytes), lung, and brain, and its stimulation generally results in vasoconstriction. Activation of ETA receptors can be stimulated by binding of ET-1 and ET-2, but not ET-3. triggering the release of vasorelaxive factors such as nitric oxide (NO) and prostanoids from endothelial cells. Human ETB receptors are primarily expressed in endothelial cells lining the vessel walls of the lungs, heart, and brain, and in contrast to ETA receptors, stimulation generally results in transient vasodilation. Activation of ETB receptors can be stimulated by binding of all three endothelins, triggering the release of vasorelaxive

UOM: 1 * 100 µG

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Numero del catalogo: (ENZOALX804494C100)

Proveedor: ENZO LIFE SCIENCES

Descripción: Caspase-11 not only activates caspase-1, that is required for the maturation of proinflammatory cytokines such as interleukin-1 (IL-1) and interleukin-18 (IL-18), but also activates caspase-3, leading to cellular apoptosis under pathological conditions. In most cells, caspase-11 is only expressed upon induction with pro-inflammatory stimuli. Caspase-11 is an essential mediator of endotoxic shock and caspase-11-deficient mice are resistant to endotoxic shock. LPS-induced caspase-11 regulates lymphocyte apoptosis by activating both caspase-3 and caspase-7. Human caspase-4, thought to be the homolog of mouse caspase-11, may be an effective therapeutic target for treatment of septic shock.

UOM: 1 * 100 µG

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