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Host
0
Species Reactivity
0
Species Reactivity
0
Conjugate
0
Conjugate
0
Compatible Species
0
Conjugate
0

验证数据展示

  • WB analysis using 20717-1-AP (same clone as 20717-1-PBS)

    WB analysis using 20717-1-AP (same clone as 20717-1-PBS)

    Various lysates were subjected to SDS PAGE followed by western blot with 20717-1-AP (ESPN antibody) at dilution of 1:1000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 20717-1-PBS in a different storage buffer formulation.

  • IHC staining of human ovary cancer using 20717-1-AP (same clone as 20717-1-PBS)

    IHC staining of human ovary cancer using 20717-1-AP (same clone as 20717-1-PBS)

    Immunohistochemical analysis of paraffin-embedded human ovary cancer tissue slide using 20717-1-AP (ESPN antibody) at dilution of 1:200 (under 20x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 20717-1-PBS in a different storage buffer formulation.

ESPN Polyclonal antibody, PBS Only

ESPN Polyclonal Antibody for WB, IHC, Indirect ELISA
Cat No. 20717-1-PBS

产品说明书

宿主/亚型

Rabbit / IgG

种属反应性

human, mouse, rat

应用

WB, IHC, Indirect ELISA

别名

LP2654, Espin, DFNB36

缓冲液配方:  PBS Only
PBS and Azide
PBS Only
偶联物:  Unconjugated
规格价格库存

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产品信息

20717-1-PBS targets ESPN in WB, IHC, Indirect ELISA applications and shows reactivity with human, mouse, rat samples.

经测试应用 WB, IHC, Indirect ELISA Application Description
经测试反应性 human, mouse, rat
免疫原 Peptide 种属同源性预测
宿主/亚型 Rabbit / IgG
抗体类别 Polyclonal
产品类型 Antibody
全称 espin
别名 LP2654, Espin, DFNB36
计算分子量 92 kDa
观测分子量 30-33 kDa, 110 kDa
GenBank蛋白编号NM_031475
基因名称 ESPN
Gene ID (NCBI) 83715
RRIDAB_10858327
偶联类型 Unconjugated
形式 Liquid
纯化方式Antigen affinity purification
UNIPROT IDB1AK53
储存缓冲液 PBS only, pH 7.3.
储存条件Store at -80°C.
The product is shipped with ice packs. Upon receipt, store it immediately at -80°C

背景介绍

ESPN, also named as DFNB36, is a multifunctional actin-bundling protein. ESPN plays a major role in regulating the organization, dimensions, dynamics and signaling capacities of the actin filament-rich, microvillus-type specializations that mediate sensory transduction in variouS mechanosensory and chemosensory cells. Defects in ESPN are the cause of deafness autosomal recessive type 36 (DFNB36). Defects in ESPN are the cause of deafness autosomal dominant without vestibular involvement (DFNAWVI). The antibody is specific to ESPN.