E0409
モノクロナール抗EDEM3 マウス宿主抗体
~1.0 mg/mL, clone EDEM3-1, purified immunoglobulin, buffered aqueous solution
別名:
抗ER分解エンハンサー, マンノシダーゼα様3抗体
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About This Item
UNSPSCコード:
12352203
NACRES:
NA.41
結合体:
unconjugated
application:
WB
クローン:
EDEM3-1, monoclonal
化学種の反応性:
rat, mouse, human
citations:
5
テクニック:
western blot: 1-2 μg/mL using whole extract of mouse 3T3 or rat NRK cells
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由来生物
mouse
品質水準
結合体
unconjugated
抗体製品の状態
purified immunoglobulin
抗体製品タイプ
primary antibodies
クローン
EDEM3-1, monoclonal
フォーム
buffered aqueous solution
分子量
antigen ~120 kDa
化学種の反応性
rat, mouse, human
濃度
~1.0 mg/mL
テクニック
western blot: 1-2 μg/mL using whole extract of mouse 3T3 or rat NRK cells
UniProtアクセッション番号
輸送温度
dry ice
保管温度
−20°C
ターゲットの翻訳後修飾
unmodified
遺伝子情報
human ... EDEM3(80267)
mouse ... Edem3(66967)
rat ... Edem3(289085)
詳細
Monoclonal Anti-EDEM3 (mouse IgG1 isotype) is derived from the hybridoma EDEM3-1 produced by the fusion of mouse myeloma cells and splenocytes from BALB/c mice immunized with a synthetic peptide corresponding to a fragment of human EDEM3 conjugated to KLH.
Three EDEM homologs, EDEM1, EDEM2 and EDEM3 have been identified, which are transcriptionally upregulated upon ER stress by the activated IRE1/Xbp-1 branch.
アプリケーション
Monoclonal Anti-EDEM3 antibody produced in mouse has been used in immunoblotting.
生物化学的／生理学的作用
EDEM3 (ER degradation enhancer, mannosidase α-like 3), a soluble EDEM homolog, enhances glycoprotein endoplasmic reticulum-associated degradation (ERAD) and mannose trimming. EDEM3 accelerates ERAD of misfolded glycoproteins as well, but in ontrast to EDEM1, it greatly stimulates mannosidase trimming in vivo.
物理的形状
0.01 M PBS溶液(pH 7.4, 15 mMアジ化ナトリウム含有)。
免責事項
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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保管分類コード
12 - Non Combustible Liquids
WGK
nwg
引火点(°F)
Not applicable
引火点(℃)
Not applicable
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
E0409-BULK:
E0409-25UL:
E0409-VAR:
E0409-200UL:
最新バージョンのいずれかを選択してください：
Katsuyoshi Mizukami et al.
Neuropathology : official journal of the Japanese Society of Neuropathology, 34(1), 11-18 (2013-07-23)
This post mortem immunohistochemical study examined the localization and distribution of ubiquilin-1 (UBL), a shuttle protein which interacts with ubiquitin and the proteasome, in the hippocampus from Alzheimer's disease (AD) dementia cases, and age-matched cases without dementia. In Braak stages
Min Ni et al.
FEBS letters, 581(19), 3641-3651 (2007-05-08)
The field of endoplasmic reticulum (ER) stress in mammalian cells has expanded rapidly during the past decade, contributing to understanding of the molecular pathways that allow cells to adapt to perturbations in ER homeostasis. One major mechanism is mediated by
Kazuyoshi Hirao et al.
The Journal of biological chemistry, 281(14), 9650-9658 (2006-01-25)
Quality control in the endoplasmic reticulum ensures that only properly folded proteins are retained in the cell through mechanisms that recognize and discard misfolded or unassembled proteins in a process called endoplasmic reticulum-associated degradation (ERAD). We previously cloned EDEM (ER
Genetic dissection of mammalian ERAD through comparative haploid and CRISPR forward genetic screens.
Richard T Timms et al.
Nature communications, 7, 11786-11786 (2016-06-11)
The application of forward genetic screens to cultured human cells represents a powerful method to study gene function. The repurposing of the bacterial CRISPR/Cas9 system provides an effective method to disrupt gene function in mammalian cells, and has been applied
Redundant and Antagonistic Roles of XTP3B and OS9 in Decoding Glycan and Non-glycan Degrons in ER-Associated Degradation
van der Goot AT, et al.
Molecular Cell, 70(3), 516-530 e6-516-530 e6 (2018)
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