閾剁墝浼氬憳绗?span style="font-size:1.5em;color:#f21">2骞滁/div> 璁块棶閲廁 3548128 缃戝潃:vbogene.cnreagent.com 鍦ㄧ嚎鐣欒█
浜у搧鎼滅储
铔嬬櫧璐?鎶楀師/澶氳偨 >> 閲嶇粍铔嬬櫧
閲嶇粍EIF1AD铔嬬櫧
閲嶇粍EIF1AD铔嬬櫧鍥剧墖
浜よ揣鏈烔 1鍛?/span>
绱㈠彇璧勬枡鍙婃姤浠饵/span>
浜よ揣鏈烔 1鍛?/td>
浜у搧鍒悕: Recombinant Eif1ad
Recombinant eukaryotic translation initiation factor 1A domain containing protein
浜у搧浠嬬粛
鍩哄洜鍚嶏細

Eif1ad


浜у搧鍒悕锛欬p style="text-indent: 2em;">2010003J03Rik锛 AI131644锛 Eif1ad1锛 Eif1ad锛 eukaryotic translation initiation factor 1A domain containing锛 eukaryotic translation initiation factor 1A domain containing锛 probable RNA-binding protein EIF1AD锛 eukaryotic translation initiation factor 1A domain-containing protein锛 EIF1AD铔嬬櫧锛


鑳屾櫙淇℃伅锛欬div style="text-indent: 2em;">eIF1AD is a 165 amino acid protein that belongs to the eIF1AD family and contains one S1-like domain. eIF1AD localizes to nucleus and is expressed in the glioblastoma cell line U-87 MG, the embryonic kidney cell line HEK-293, the pancreatic carcinoma cell line PANC-1, the breast carcinoma cell line MCF7, the lung cancer cell line NCI-H460, and the chronic myelogenous leukemia cell line K-562. eIF1AD interacts with GAPDH and may function to reduce cell proliferation. The gene encoding eIF1AD maps to human chromosome 11q13.1. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in chromosome 11.

鏍囩锛欻is-tag
鍒嗙被锛歊ecombinant
绫诲瀷锛歅rotein
鍋惰仈鐗╋細Unconjugated
鍐呮瘨绱犳按骞筹細鎸夋壒娆★紝鍙傞槄鐡惰韩鏍囩
鎬х姸:Liquid
娴撳害锛欱atch dependent (Please refer to the vial label for the specific concentration.)
绾寲绫诲瀷锛歱urified
鍐呭惈鐗╋細涓嶅惈闃茶厫鍓侟br/>搴旂敤:Positive Control;Immunogen;SDS-PAGE;WB.
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