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Nogo B receptor Recombinant Rabbit mAb (bsm-63800R)  
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25ul/800.00元
50ul/1400.00元
100ul/2500.00元
大包装/询价
产品编号 bsm-63800R
英文名称 Nogo B receptor Recombinant Rabbit mAb
中文名称
别    名 C6orf68; CDG1AA; MGC:7199; MRD55; NgBR; TANGO14; 1600027K07Rik; D10Ertd438e; RGD1307879; NGBR_HUMAN; NUS1; Cis-prenyltransferase subunit NgBR; Nogo-B receptor (NgBR); Nuclear undecaprenyl pyrophosphate synthase 1 homolog; 2.5.1.87; NGBR_MOUSE; NUS1 dehydrodolichyl diphosphate synthase subunit; chromosome 6 open reading frame 68; nuclear undecaprenyl pyrophosphate synthase 1 homolog (S. cerevisiae); Nogo-B receptor; transport and golgi organization 14 homolog (Drosophila); Dehydrodolichyl diphosphate synthase complex subunit NUS1 (EC 2.5.1.87) (Cis-prenyltransferase subunit NgBR) (Nogo-B receptor) (NgBR) (Nuclear undecaprenyl pyrophosphate synthase 1 homolog); C6orf68 NGBR  
抗体来源 Rabbit
克隆类型 Recombinant
克 隆 号 7F1
交叉反应 Human,Mouse,Rat
产品应用 WB=1:1000-5000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
PubMed PubMed
产品介绍 This gene encodes a type I single transmembrane domain receptor, which is a subunit of cis-prenyltransferase, and serves as a specific receptor for the neural and cardiovascular regulator Nogo-B. The encoded protein is essential for dolichol synthesis and protein glycosylation. This gene is highly expressed in non-small cell lung carcinomas as well as estrogen receptor-alpha positive breast cancer cells where it promotes epithelial mesenchymal transition. This gene is associated with the poor prognosis of human hepatocellular carcinoma patients. Naturally occurring mutations in this gene cause a congenital disorder of glycosylation and are associated with epilepsy. A knockout of the orthologous gene in mice causes embryonic lethality before day 6.5. Pseudogenes of this gene have been defined on chromosomes 13 and X. [provided by RefSeq, May 2017]

SWISS:
Q96E22

Gene ID:
116150

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