NeoBiotechnologies

Dystrophin (DMD) (Marker of Duchenne and Becker Muscular Dystrophy) Monoclonal Antibody (DMD/3241)

Name: Dystrophin (DMD) (Marker of Duchenne and Becker Muscular Dystrophy) Monoclonal Antibody (DMD\/3241)
Brand: NeoBiotechnologies
SKU: 1756-MSM1-P1ABX

查看其他32个Dystrophin抗体

说明书

实验方案

问题与答案

技术支持

说明书

实验方案

问题与答案

技术支持

说明书

实验方案

问题与答案

技术支持

抗体检测数据 (4)

Dystrophin (DMD) (Marker of Duchenne and Becker Muscular Dystrophy) Antibody in Immunohistochemistry (Paraffin) (IHC (P))

图: 1 / 4

Dystrophin (DMD) (Marker of Duchenne and Becker Muscular Dystrophy) Antibody (1756-MSM1-P1ABX) in IHC (P)

Formalin-fixed, paraffin-embedded human skeletal muscle stained with Dystrophin Monospecific Mouse Monoclonal Antibody (DMD/3241).

Dystrophin (DMD) (Marker of Duchenne and Becker Muscular Dystrophy) Antibody in Peptide array (ARRAY)

Dystrophin (DMD) (Marker of Duchenne and Becker Muscular Dystrophy) Antibody in SDS-PAGE (SDS-PAGE)

Product Image Gallery

Immunogen image

Immunogen Image Dystrophin (DMD) (Marker of Duchenne and Becker Muscular Dystrophy) Monoclonal Antibody (DMD/3241)

产品信息

1756-MSM1-P1ABX

应用

建议稀释比

已发表文章

免疫组化（石蜡） (IHC (P))

Assay-dependent

免疫组织化学（多聚甲醛固定） (IHC (PFA))

1-2 µg/mL

酶联免疫吸附实验 (ELISA)

Assay-dependent

肽阵列 (Array)

Assay-dependent

产品规格

种属反应

Human

宿主/亚型

Mouse / IgG1, kappa

分类

Monoclonal

类型

Antibody

克隆号

DMD/3241

抗原

A recombinant fragment (around aa 114-263) of human DMD protein.

查看免疫原

偶联物

Unconjugated Unconjugated Unconjugated

形式

Liquid

浓度

1 mg/mL

纯化类型

Protein A/G

保存液

PBS, pH 7.4

内含物

no preservative

保存条件

-20°C, Avoid Freeze/Thaw Cycles

运输条件

Ambient (domestic); Wet ice (international)

靶标信息

Dystrophin is the 427kDa protein product of the DMB/BMD gene located on the X chromosome at position Xp21. Western blotting and immunohistochemistry are the two established methods for the detection of abnormalities of dystrophin expression in muscle biopsies. Dystrophin abnormalities are thought to occur in 100% of patients with DMD/BMD, although genetic abnormalities may only be detected in up to 65% of cases.

仅用于科研。不用于诊断过程。未经明确授权不得转售。