Anticorps
Numéro de catalogue:
(USBI035754)
Fournisseur:
US Biological
Description:
Anti-FOXP3 Rabbit Polyclonal Antibody
UOM:
1 * 200 µl
Numéro de catalogue:
(USBI035760-BIOTIN)
Fournisseur:
US Biological
Description:
Anti-FPR1 Rabbit Polyclonal Antibody (Biotin)
UOM:
1 * 200 µl
Numéro de catalogue:
(USBI035761)
Fournisseur:
US Biological
Description:
Anti-FPR3 Rabbit Polyclonal Antibody
UOM:
1 * 200 µl
Numéro de catalogue:
(USBI035754-BIOTIN)
Fournisseur:
US Biological
Description:
Anti-FOXP3 Rabbit Polyclonal Antibody (Biotin)
UOM:
1 * 200 µl
Numéro de catalogue:
(USBI035750)
Fournisseur:
US Biological
Description:
Anti-FOXO3 Rabbit Polyclonal Antibody
UOM:
1 * 200 µl
Numéro de catalogue:
(USBIS8022-02A)
Fournisseur:
US Biological
Description:
Anti-SULT2A Rabbit Polyclonal Antibody
UOM:
1 * 200 µl
Numéro de catalogue:
(USBIS8022-03B2)
Fournisseur:
US Biological
Description:
Anti-SULT1A3 Mouse Monoclonal Antibody [clone: 10K350]
UOM:
1 * 1 EA
Numéro de catalogue:
(USBIS8016-01)
Fournisseur:
US Biological
Description:
Anti-Sulfapyridine Sheep Polyclonal Antibody
UOM:
1 * 100 µl
Numéro de catalogue:
(USBI044334)
Fournisseur:
US Biological
Description:
Anti-ZNF691 Rabbit Polyclonal Antibody
UOM:
1 * 200 µl
Numéro de catalogue:
(USBIS8022-03B1)
Fournisseur:
US Biological
Description:
Anti-SULT1A3 Mouse Monoclonal Antibody [clone: 10K349]
UOM:
1 * 1 EA
Numéro de catalogue:
(USBIS8022-03F1)
Fournisseur:
US Biological
Description:
Anti-SULT1C2 Rabbit Polyclonal Antibody
UOM:
1 * 200 µl
Numéro de catalogue:
(BOSSBS-11728R)
Fournisseur:
Bioss
Description:
Epilepsy affects about 0.5% of the world’s population and has a large genetic component. Epilepsy results from an electrical hyperexcitability in the central nervous system. Potassium channels are important regulators of electrical signaling, determining the firing properties and responsiveness of a variety of neurons. Benign familial neonatal convulsions (BFNC), an autosomal dominant epilepsy of infancy, has been shown to be caused by mutations in the KCNQ2 or the KCNQ3 potassium channel genes. KCNQ2 and KCNQ3 are voltage-gated potassium channel proteins with six putative transmembrane domains. Both proteins display a broad distribution within the brain, with expression patterns that largely overlap.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-11717R)
Fournisseur:
Bioss
Description:
Members of the C1q superfamily have diverse functions that are related to cell adhesion and basement membrane components. CTRP5 (Complement C1q tumor necrosis factor-related protein 5) is a 243 amino acid secreted and membrane-associated protein that contains a collagen-like domain and a C1q domain. CTRP5 is a short-chain collagen that is expressed in retinal pigment epithelium as well as brain, lung, liver and placenta. By forming an extracellular hexagonal lattice, CTRP5 facilitates the adhesion of basal retinal pigment epithelium to Bruch’s membrane, the innermost layer of the choroid. A mutation within the C1q domain of CTRP5 results in abnormal high molecular weight aggregate formation, which alters its structure and interactions. This mutation may result in the presentation of late-onset retinal degeneration (LORD), an autosomal dominant disorder that is characterized by punctate yellow-white deposits in the retinal fundus and night blindness.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-11719R)
Fournisseur:
Bioss
Description:
Calcyon is a single transmembrane protein that interacts with D1 dopamine receptors. Dopamine is a neurotransmitter that regulates synaptic transmission involved in learning and memory. D1 receptors, the most abundant dopamine receptor in the central nervous system, appear to modulate the activity of D2 dopamine receptors, mediate various behavioural responses, and regulate neuron growth and differentiation. Calcyon is present in neuronal cell bodies and processes of the cortex and hippocampus, and it is especially abundant in pyramidal neurons. Interaction of Calcyon with D1 receptors results in a release of intracellular calcium.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-10529R)
Fournisseur:
Bioss
Description:
This gene encodes a member of the semicarbazide-sensitive amine oxidase family. Copper amine oxidases catalyze the oxidative conversion of amines to aldehydes in the presence of copper and quinone cofactor. The encoded protein is localized to the cell surface, has adhesive properties as well as monoamine oxidase activity, and may be involved in leukocyte trafficking. Alterations in levels of the encoded protein may be associated with many diseases, including diabetes mellitus. A pseudogene of this gene has been described and is located approximately 9-kb downstream on the same chromosome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2013]
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-13383R)
Fournisseur:
Bioss
Description:
Glucoamylase is an important industrial enzyme used in saccharification steps in both starch enzymatic conversion and in alcohol production. The catalytic domain degrades oligosaccharides from the non reducing end, releasing glucose, and the starch domain binds the enzyme to raw starch and to the cell wall.
UOM:
1 * 100 µl
Appel de prix
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