多克隆抗体

NPBW2 rabbit Polyclonal Antibody

NPBW2抗体
NPBW2抗体应用:WB 1:500-2000 ELISA 1:5000-20000neuropeptides B/W receptor 2(NPBWR2) Homo sapiens The protein encoded by this gene is an integral membrane protein and G protein-coupled receptor. The encoded protein is similar in sequence to another G protein-coupled receptor (GPR7), and it is structurally similar to opioid and somatostatin receptors. This protein binds neuropeptides B and W. This gene is intronless and is expressed primarily in the frontal cortex of the brain. [provided by RefSeq, Jul 2008],

NPFF1 rabbit Polyclonal Antibody

NPFF1抗体
NPFF1抗体应用:WB 1:500-2000 ELISA 1:5000-20000function:Receptor for NPAF (A-18-F-amide) and NPFF (F-8-F-amide) neuropeptides, also known as morphine-modulating peptides. Can also be activated by a variety of naturally occurring or synthetic FMRF-amide like ligands. This receptor mediates its action by association with G proteins that activate a phosphatidylinositol-calcium second messenger system.,similarity:Belongs to the G-protein coupled receptor 1 family.,

NPFF2 rabbit Polyclonal Antibody

NPFF2抗体
NPFF2抗体应用:WB 1:500-2000 ELISA 1:5000-20000neuropeptide FF receptor 2(NPFFR2) Homo sapiens This gene encodes a member of a subfamily of G-protein-coupled neuropeptide receptors. This protein is activated by the neuropeptides A-18-amide (NPAF) and F-8-amide (NPFF) and may function in pain modulation and regulation of the opioid system. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2009],

NPHP1 rabbit Polyclonal Antibody

NPHP1抗体
NPHP1抗体应用:WB 1:500-2000 ELISA 1:5000-20000nephrocystin 1(NPHP1) Homo sapiens This gene encodes a protein with src homology domain 3 (SH3) patterns. This protein interacts with Crk-associated substrate, and it appears to function in the control of cell division, as well as in cell-cell and cell-matrix adhesion signaling, likely as part of a multifunctional complex localized in actin- and microtubule-based structures. Mutations in this gene cause familial juvenile nephronophthisis type 1, a kidney disorder involving both tubules and glomeruli. Defects in this gene are also associated with Senior-Loken syndrome type 1, also referred to as juvenile nephronophthisis with Leber amaurosis, which is characterized by kidney and eye disease, and with Joubert syndrome type 4, which is characterized by cerebellar ataxia, oculomotor apraxia, psychomotor delay and neonatal breathing abnormalities, sometimes including retinal dystrophy and renal disease. Multiple transcript variants encoding diffe

NPIP rabbit Polyclonal Antibody

NPIP抗体
NPIP抗体应用:WB 1:500-2000 ELISA 1:5000-20000similarity:Belongs to the NPIP family.,similarity:Contains 1 GPS domain.,subcellular location:Colocalizes with nuclear pore complex protein NUP62.,subunit:May associate with the nuclear pore complex.,tissue specificity:Widely expressed.,

NPL4 rabbit Polyclonal Antibody

NPL4抗体
NPL4抗体应用:WB 1:500-2000 ELISA 1:5000-20000domain:Binds ubiquitinated proteins via its RanBP2-type zinc finger.,function:The ternary complex containing UFD1L, VCP and NPLOC4 binds ubiquitinated proteins and is necessary for the export of misfolded proteins from the ER to the cytoplasm, where they are degraded by the proteasome. The NPLOC4-UFD1L-VCP complex regulates spindle disassembly at the end of mitosis and is necessary for the formation of a closed nuclear envelope.,pathway:Protein degradation; proteasomal ubiquitin-dependent pathway.,similarity:Belongs to the NPL4 family.,similarity:Contains 1 RanBP2-type zinc finger.,subcellular location:Associated with the endoplasmic reticulum and nuclear.,subunit:Heterodimer with UFD1L. The heterodimer binds ubiquitinated proteins. The heterodimer binds to VCP and inhibits Golgi membrane fusion.,tissue specificity:Expressed at highest levels in brain, heart, skeletal muscle, kidney and fetal liver.,

NPNT rabbit Polyclonal Antibody

NPNT抗体
NPNT抗体应用:WB 1:500-2000

NPRL3 rabbit Polyclonal Antibody

NPRL3抗体
NPRL3抗体应用:WB 1:500-2000 The function of the encoded protein is not known. [provided by RefSeq, Aug 2011],

NPSR1 rabbit Polyclonal Antibody

NPSR1抗体
NPSR1抗体应用:WB 1:500-2000 ELISA 1:5000-20000neuropeptide S receptor 1(NPSR1) Homo sapiens This gene encodes a member of the vasopressin/oxytocin subfamily of G protein-coupled receptors. The encoded membrane protein acts as a receptor for neuropeptide S and affects a variety of cellular processes through its signaling. Increased expression of this gene in ciliated cells of the respiratory epithelium and in bronchial smooth muscle cells is associated with asthma. Polymorphisms in this gene have also been associated with asthma susceptibility, panic disorders, inflammatory bowel disease, and rheumatoid arthritis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014],

NPT2A rabbit Polyclonal Antibody

NPT2A抗体
NPT2A抗体应用:WB 1:500-2000 ELISA 1:5000-20000solute carrier family 34 member 1(SLC34A1) Homo sapiens This gene encodes a member of the type II sodium-phosphate cotransporter family. Mutations in this gene are associated with hypophosphatemia nephrolithiasis/osteoporosis 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2009],
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