anti-Filamin antibody [FLMN01 (PM6/317)]

Key features and details

  • 产品描述: Mouse Monoclonal antibody [FLMN01 (PM6/317)] recognizes Filamin
  • 反应物种: Hu, Ms, Rat, Chk, Gpig, Rb
  • 应用: ELISA, IHC, IHC-P, WB
  • 宿主: Mouse
  • 克隆: Monoclonal
  • 克隆号: FLMN01 (PM6/317)
  • 同位型: IgG1
  • 靶点名称: Filamin
  • 抗原: Platelet filamin
  • Brand:
CAT.NO. : ARG62492
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Product Details
概述
产品描述Mouse Monoclonal antibody [FLMN01 (PM6/317)] recognizes Filamin
反应物种Hu, Ms, Rat, Chk, Gpig, Rb
应用ELISA, IHC, IHC-P, WB
宿主Mouse
克隆Monoclonal
克隆号FLMN01 (PM6/317)
同位型IgG1
靶点名称Filamin
抗原Platelet filamin
偶联标记Un-conjugated
別名Endothelial actin-binding protein; ABP-280; XMVD; ABPX; Actin-binding protein 280; FLN1; MNS; OPD1; XLVD; OPD2; OPD; Non-muscle filamin; CSBS; Filamin-A; FLN-A; FLN; NHBP; Filamin-1; FMD; Alpha-filamin; CVD1
应用说明
应用说明WB: 1-2 ug/ml
ELISA 1/100 - 1/2000
IHC: 1/10-1/500
IHC-P: 1-2 ug/ml
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
属性
形式Liquid
纯化Protein G purified
缓冲液10mM PBS (pH 7.4), 0.2% BSA and 0.09% Sodium azide
抗菌剂0.09% Sodium azide
稳定剂0.2% BSA
浓度0.2 mg/ml
存放说明For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
注意事项For laboratory research only, not for drug, diagnostic or other use.
生物信息
数据库连接

GeneID: 192176 Mouse FLNA

GeneID: 2316 Human FLNA

Swiss-port # P21333 Human Filamin-A

Swiss-port # Q8BTM8 Mouse Filamin-A

基因名称FLNA
全名filamin A, alpha
背景介绍The protein encoded by this gene is an actin-binding protein that crosslinks actin filaments and links actin filaments to membrane glycoproteins. The encoded protein is involved in remodeling the cytoskeleton to effect changes in cell shape and migration. This protein interacts with integrins, transmembrane receptor complexes, and second messengers. Defects in this gene are a cause of several syndromes, including periventricular nodular heterotopias (PVNH1, PVNH4), otopalatodigital syndromes (OPD1, OPD2), frontometaphyseal dysplasia (FMD), Melnick-Needles syndrome (MNS), and X-linked congenital idiopathic intestinal pseudoobstruction (CIIPX). Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2009]
生物功能Promotes orthogonal branching of actin filaments and links actin filaments to membrane glycoproteins. Anchors various transmembrane proteins to the actin cytoskeleton and serves as a scaffold for a wide range of cytoplasmic signaling proteins. Interaction with FLNA may allow neuroblast migration from the ventricular zone into the cortical plate. Tethers cell surface-localized furin, modulates its rate of internalization and directs its intracellular trafficking (By similarity). Involved in ciliogenesis. [UniProt]
细胞定位Cytoplasm; cell cortex
研究领域Signaling Transduction antibody
预测分子量281 kDa
翻译后修饰Phosphorylation at Ser-2152 is negatively regulated by the autoinhibited conformation of filamin repeats 19-21. Ligand binding induces a conformational switch triggering phosphorylation at Ser-2152 by PKA.
Phosphorylation extent changes in response to cell activation.
Polyubiquitination in the CH1 domain by a SCF-like complex containing ASB2 leads to proteasomal degradation. Prior dissociation from actin may be required to expose the target lysines (PubMed:24052262). Ubiquitinated in endothelial cells by RNF213 downstream of the non-canonical Wnt signaling pathway, leading to its degradation by the proteasome (PubMed:26766444).
参考文献

克隆号文献

Cyclin B1/Cdk1 binds and phosphorylates Filamin A and regulates its ability to cross-link actin.

WB / Human

Cukier IH et al.
FEBS Lett.,  (2007)

publication_link

 

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