多克隆抗体

SCAR3 rabbit Polyclonal Antibody

SCAR3抗体
SCAR3抗体应用:WB 1:500-2000 ELISA 1:5000-20000scavenger receptor class A member 3(SCARA3) Homo sapiens This gene encodes a macrophage scavenger receptor-like protein. This protein has been shown to deplete reactive oxygen species, and thus play an important role in protecting cells from oxidative stress. The expression of this gene is induced by oxidative stress. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008],

SCAR5 rabbit Polyclonal Antibody

SCAR5抗体
SCAR5抗体应用:WB 1:500-2000 ELISA 1:5000-20000function:Ferritin receptor that mediates non-transferrin-dependent delivery of iron. Mediates cellular uptake of ferritin-bound iron by stimulating ferritin endocytosis from the cell surface with consequent iron delivery within the cell. Delivery of iron to cells by ferritin is required for the development of specific cell types, suggesting the existence of cell type-specific mechanisms of iron traffic in organogenesis, which alternatively utilize transferrin or non-transferrin iron delivery pathways. Ferritin mediates iron uptake in capsule cells of the developing kidney. Binds preferrentially ferritin light chain (FTL) compared to heavy chain (FTH1).,similarity:Belongs to the SCARA5 family.,similarity:Contains 1 collagen-like domain.,similarity:Contains 1 SRCR domain.,subunit:Homotrimer.,

SCG1 rabbit Polyclonal Antibody

SCG1抗体
SCG1抗体应用:WB 1:500-2000 ELISA 1:5000-20000chromogranin B(CHGB) Homo sapiens This gene encodes a tyrosine-sulfated secretory protein abundant in peptidergic endocrine cells and neurons. This protein may serve as a precursor for regulatory peptides. [provided by RefSeq, Jan 2009],

SCLY rabbit Polyclonal Antibody

SCLY抗体
SCLY抗体应用:WB 1:500-2000 Selenocysteine lyase (SCLY; EC 4.4.1.16) catalyzes the pyridoxal 5-prime phosphate-dependent conversion of L-selenocysteine to L-alanine and elemental selenium (Mihara et al., 2000 [PubMed 10692412]).[supplied by OMIM, Mar 2008],

SCN1A rabbit Polyclonal Antibody

SCN1A抗体
SCN1A抗体应用:WB 1:500-2000 ELISA 1:5000-20000sodium voltage-gated channel alpha subunit 1(SCN1A) Homo sapiens Voltage-dependent sodium channels are heteromeric complexes that regulate sodium exchange between intracellular and extracellular spaces and are essential for the generation and propagation of action potentials in muscle cells and neurons. Each sodium channel is composed of a large pore-forming, glycosylated alpha subunit and two smaller beta subunits. This gene encodes a sodium channel alpha subunit, which has four homologous domains, each of which contains six transmembrane regions. Allelic variants of this gene are associated with generalized epilepsy with febrile seizures and epileptic encephalopathy. Alternative splicing results in multiple transcript variants. The RefSeq Project has decided to create four representative RefSeq records. Three of the transcript variants are supported by experimental evidence and the fourth contains alternate 5' untranslated exons, th

SCN1B rabbit Polyclonal Antibody

SCN1B抗体
SCN1B抗体应用:WB 1:500-2000 ELISA 1:5000-20000sodium voltage-gated channel beta subunit 1(SCN1B) Homo sapiens Voltage-gated sodium channels are heteromeric proteins that function in the generation and propagation of action potentials in muscle and neuronal cells. They are composed of one alpha and two beta subunits, where the alpha subunit provides channel activity and the beta-1 subunit modulates the kinetics of channel inactivation. This gene encodes a sodium channel beta-1 subunit. Mutations in this gene result in generalized epilepsy with febrile seizures plus, Brugada syndrome 5, and defects in cardiac conduction. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009],

SCN3A rabbit Polyclonal Antibody

SCN3A抗体
SCN3A抗体应用:WB 1:500-2000 ELISA 1:5000-20000sodium voltage-gated channel alpha subunit 3(SCN3A) Homo sapiens Voltage-gated sodium channels are transmembrane glycoprotein complexes composed of a large alpha subunit with 24 transmembrane domains and one or more regulatory beta subunits. They are responsible for the generation and propagation of action potentials in neurons and muscle. This gene encodes one member of the sodium channel alpha subunit gene family, and is found in a cluster of five alpha subunit genes on chromosome 2. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008],

SCN8A rabbit Polyclonal Antibody

SCN8A抗体
SCN8A抗体应用:WB 1:500-2000 ELISA 1:5000-20000sodium voltage-gated channel alpha subunit 8(SCN8A) Homo sapiens This gene encodes a member of the sodium channel alpha subunit gene family. The encoded protein forms the ion pore region of the voltage-gated sodium channel. This protein is essential for the rapid membrane depolarization that occurs during the formation of the action potential in excitable neurons. Mutations in this gene are associated with mental retardation, pancerebellar atrophy and ataxia. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2010],

SCNAA rabbit Polyclonal Antibody

SCNAA抗体
SCNAA抗体应用:WB 1:500-2000 ELISA 1:5000-20000sodium voltage-gated channel alpha subunit 10(SCN10A) Homo sapiens The protein encoded by this gene is a tetrodotoxin-resistant voltage-gated sodium channel alpha subunit. The properties of the channel formed by the encoded transmembrane protein can be altered by interaction with different beta subunits. This protein may be involved in the onset of pain associated with peripheral neuropathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014],

SCNBA rabbit Polyclonal Antibody

SCNBA抗体
SCNBA抗体应用:WB 1:500-2000 ELISA 1:5000-20000sodium voltage-gated channel alpha subunit 11(SCN11A) Homo sapiens Voltage-gated sodium channels are membrane protein complexes that play a fundamental role in the rising phase of the action potential in most excitable cells. Alpha subunits, such as SCN11A, mediate voltage-dependent gating and conductance, while auxiliary beta subunits regulate the kinetic properties of the channel and facilitate membrane localization of the complex. Aberrant expression patterns or mutations of alpha subunits underlie a number of disorders. Each alpha subunit consists of 4 domains connected by 3 intracellular loops; each domain consists of 6 transmembrane segments and intra- and extracellular linkers.[supplied by OMIM, Apr 2004],
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