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1 µg/mL was sufficient for detection of KDEL receptor in 20 µg monkey Vero cell lysate by colorimetric immunoblot analysis using Goat Anti-Mouse IgG:AP as the secondary.|Detects approximately 25kDa.
KDELR1 (KDEL Endoplasmic Reticulum Protein Retention Receptor 1) is a Protein Coding gene. Diseases associated with KDELR1 include Syndromic X-Linked Intellectual Disability 94 and Myopathy, Centronuclear, 1. Among its related pathways are Transport to the Golgi and subsequent modification and Activation of cAMP-Dependent PKA. Gene Ontology (GO) annotations related to this gene include ER retention sequence binding and KDEL sequence binding. An important paralog of this gene is KDELR2.
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Protein Aliases: ER lumen protein retaining receptor 1; ER lumen protein-retaining receptor 1; KDEL (Lys-Asp-Glu-Leu) endoplasmic reticulum protein retention receptor 1; KDEL endoplasmic reticulum protein retention receptor 1; KDEL receptor 1; Putative MAPK-activating protein PM23
Gene Aliases: 8030486F04Rik; AW215843; BOS_17737; ERD2; ERD2.1; HDEL; I79_020931; KDELR; KDELR1; PM23
UniProt ID: (Human) P24390, (Bovine) P33946, (Mouse) Q99JH8, (Rat) Q569A6
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