anti-Dysferlin antibody

Key features and details

  • 产品描述: Rabbit Polyclonal antibody recognizes Dysferlin
  • 反应物种: Hu, Ms
  • 应用: ICC/IF, IHC-P, WB
  • 宿主: Rabbit
  • 克隆: Polyclonal
  • 同位型: IgG
  • 靶点名称: Dysferlin
  • 抗原物种: Human
  • 抗原: Synthetic peptide derived from Human Dysferlin.
  • Brand:
CAT.NO. : ARG43171
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Product Details
概述
产品描述Rabbit Polyclonal antibody recognizes Dysferlin
反应物种Hu, Ms
应用ICC/IF, IHC-P, WB
宿主Rabbit
克隆Polyclonal
同位型IgG
靶点名称Dysferlin
抗原物种Human
抗原Synthetic peptide derived from Human Dysferlin.
偶联标记Un-conjugated
別名FER1L1; Dystrophy-associated fer-1-like protein; Fer-1-like protein 1; LGMD2B; MMD1; Dysferlin
应用说明
应用建议
应用推荐稀释比
ICC/IF1:50 - 1:200
IHC-P1:50 - 1:200
WB1:500 - 1:1000
应用说明* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
阳性对照Mouse skeletal muscle
实际分子量~ 270 kDa
属性
形式Liquid
纯化Affinity purified.
缓冲液PBS (pH 7.4), 150 mM NaCl, 0.02% Sodium azide and 50% Glycerol.
抗菌剂0.02% Sodium azide
稳定剂50% Glycerol
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. 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: 26903 Mouse DYSF

GeneID: 8291 Human DYSF

Swiss-port # O75923 Human Dysferlin

Swiss-port # Q9ESD7 Mouse Dysferlin

基因名称DYSF
全名dysferlin
背景介绍The protein encoded by this gene belongs to the ferlin family and is a skeletal muscle protein found associated with the sarcolemma. It is involved in muscle contraction and contains C2 domains that play a role in calcium-mediated membrane fusion events, suggesting that it may be involved in membrane regeneration and repair. In addition, the protein encoded by this gene binds caveolin-3, a skeletal muscle membrane protein which is important in the formation of caveolae. Specific mutations in this gene have been shown to cause autosomal recessive limb girdle muscular dystrophy type 2B (LGMD2B) as well as Miyoshi myopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2008]
生物功能Key calcium ion sensor involved in the Ca(2+)-triggered synaptic vesicle-plasma membrane fusion. Plays a role in the sarcolemma repair mechanism of both skeletal muscle and cardiomyocytes that permits rapid resealing of membranes disrupted by mechanical stress (By similarity). [UniProt]
细胞定位Cell membrane, sarcolemma. Cytoplasmic vesicle membrane. Cell membrane. Note=Colocalizes, during muscle differentiation, with BIN1 in the T-tubule system of myotubules and at the site of contact between two myotubes or a myoblast and a myotube. Wounding of myotubes led to its focal enrichment to the site of injury and to its relocalization in a Ca(2+)-dependent manner toward the plasma membrane. Colocalizes with AHNAK, AHNAK2 and PARVB at the sarcolemma of skeletal muscle. [UniProt]
预测分子量237 kDa
检测图片 (1)
  • ARG43171 anti-Dysferlin antibody WB image

    Western blot: Mouse skeletal muscle lysate stained with ARG43171 anti-Dysferlin antibody.

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