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验证数据展示

  • IHC staining of mouse brain using 15490-1-AP

    IHC staining of mouse brain using 15490-1-AP

    Immunohistochemical analysis of paraffin-embedded mouse brain tissue slide using 15490-1-AP (SCNM1 antibody) at dilution of 1:200 (under 10x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0).

  • IHC staining of mouse brain using 15490-1-AP

    IHC staining of mouse brain using 15490-1-AP

    Immunohistochemical analysis of paraffin-embedded mouse brain tissue slide using 15490-1-AP (SCNM1 antibody) at dilution of 1:200 (under 40x lens). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0).

SCNM1 Polyclonal antibody

SCNM1 Polyclonal Antibody for IHC, ELISA
Cat No. 15490-1-AP

产品说明书

宿主/亚型

Rabbit / IgG

种属反应性

human, mouse, rat

应用

IHC, ELISA

别名

SCNM1, sodium channel modifier 1

缓冲液配方:  PBS and Azide
PBS and Azide
偶联物:  Unconjugated
Unconjugated
规格: 

-/ -

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经过测试的应用

Positive IHC detected inmouse brain tissue
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0

推荐稀释比

应用推荐稀释比
Immunohistochemistry (IHC)IHC : 1:50-1:500
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

产品信息

15490-1-AP targets SCNM1 in IHC, ELISA applications and shows reactivity with human, mouse, rat samples.

经测试应用 IHC, ELISA Application Description
经测试反应性 human, mouse, rat
免疫原 SCNM1 fusion protein Ag7854 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 sodium channel modifier 1
别名 SCNM1, sodium channel modifier 1
计算分子量 26 kDa
GenBank蛋白编号BC000264
基因名称 SCNM1
Gene ID (NCBI) 79005
RRIDAB_2184357
偶联类型 Unconjugated
形式 Liquid
纯化方式Antigen affinity purification
UNIPROT IDQ9BWG6
储存缓冲液 PBS with 0.02% sodium azide and 50% glycerol , pH 7.3
储存条件Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

背景介绍

SCNM1 is located at chromosome 1p21 which may contribute to human inherited dystonia. SCNM1 determines the proportion of correctly spliced transcripts and hence disease severity. It plays a role in RNA splicing, possibly contributing to the recognition of non-consensus donor sites.

实验方案

Product Specific Protocols
IHC protocol for SCNM1 antibody 15490-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols