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GRP78 BiP抗體應用：WB 1:500-2000,IHC-p 1:500-200, ELISA 1:10000-20000 heat shock protein family A (Hsp70) member 5(HSPA5) Homo sapiens The protein encoded by this gene is a member of the heat shock protein 70 (HSP70) family. It is localized in the lumen of the endoplasmic reticulum (ER), and is involved in the folding and assembly of proteins in the ER. As this protein interacts with many ER proteins, it may play a key role in monitoring protein transport through the cell.[provided by RefSeq, Sep 2010],

GRPE1抗體應用：WB 1:500-2000

GRPE2抗體應用：WB 1:500-2000

GRSF1抗體應用：WB 1:500-2000 The protein encoded by this gene is a cellular protein that binds RNAs containing the G-rich element. The protein is localized in the cytoplasm, and has been shown to stimulate translation of viral mRNAs in vitro. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008],

GRTP1抗體應用：Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. function:May act as a GTPase-activating protein for Rab family protein(s).,similarity:Contains 1 Rab-GAP TBC domain.,

GS28抗體應用：Western Blot: 1/500 - 1/2000. ELISA: 1/10000. golgi SNAP receptor complex member 1(GOSR1) Homo sapiens This gene encodes a trafficking membrane protein which transports proteins among the endoplasmic reticulum and the Golgi and between Golgi compartments. This protein is considered an essential component of the Golgi SNAP receptor (SNARE) complex. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008],

GSAS1抗體應用：WB 1:500-2000

GSC抗體應用：IHC-p 1:50-200, ELISA 1:10000-20000 goosecoid homeobox(GSC) Homo sapiens This gene encodes a member of the bicoid subfamily of the paired (PRD) homeobox family of proteins. The encoded protein acts as a transcription factor and may be autoregulatory. A similar protein in mice plays a role in craniofacial and rib cage development during embryogenesis. [provided by RefSeq, Jul 2008],

GSC2抗體應用：Western Blot: 1/500 - 1/2000. ELISA: 1/20000. goosecoid homeobox 2(GSC2) Homo sapiens Goosecoidlike (GSCL), a homeodomain-containing gene, resides in the critical region for VCFS/DGS on 22q11. Velocardiofacial syndrome (VCFS) is a developmental disorder characterized by conotruncal heart defects, craniofacial anomalies, and learning disabilities. VCFS is phenotypically related to DiGeorge syndrome (DGS) and both syndromes are associated with hemizygous 22q11 deletions. Because many of the tissues and structures affected in VCFS/DGS derive from the pharyngeal arches of the developing embryo, it is believed that haploinsufficiency of a gene involved in embryonic development may be responsible for its etiology. The gene is expressed in a limited number of adult tissues, as well as in early human development. [provided by RefSeq, Jul 2008],

GSG1抗體應用：WB 1:500-2000