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MAB1645

Anti-Dystrophin Antibody

CHEMICON®, mouse monoclonal, 1808

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关于此项目

UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41
Clone:
1808, monoclonal
Species reactivity:
chicken, mouse, rat, human
Application:
IHC, WB
Citations:
11
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产品名称

肌营养不良蛋白抗体，克隆1808, clone 1808, Chemicon®, from mouse

biological source

mouse

Quality Level

100

antibody form

purified antibody

antibody product type

primary antibodies

clone

1808, monoclonal

species reactivity

chicken, mouse, rat, human

manufacturer/tradename

Chemicon®

technique(s)

immunohistochemistry: suitable, western blot: suitable

isotype

IgG1

NCBI accession no.

NM_000109.2, NM_004006.1, NM_004007.1, NM_004009.2, NM_004010.2, NM_004011.2, NM_004012.2, NM_004013.1, NM_004014.1, NM_004015.1, NM_004016.1, NM_004017.1, NM_004018.1, NM_004019.2, NM_004020.1, NM_004021.1, NM_004022.1, NM_004023.1

UniProt accession no.

P11532

shipped in

dry ice

target post-translational modification

unmodified

Gene Information

human ... DMD(1756)

Immunogen

从电鳐属突触后膜提取的外周膜蛋白。

Application

肌营养不良蛋白抗体（克隆1808）可检测肌营养不良蛋白水平 & 已发表 & 经验证可用于 WB、IH。
蛋白质印迹

免疫组化

最佳工作稀释度必须由最终用户确定。

Biochem/physiol Actions

通过蛋白质印迹，MAB1645可识别相对分子量为300 kD的单一蛋白。可与哺乳动物骨骼肌肌营养不良蛋白反应。无法对mdx小鼠肌肉进行染色。可标记正常人体肌肉，但无法标记杜氏肌肉。

染色模式：

在正常小鼠膈肌冷冻切片上，MAB1645可对整个肌膜进行强免疫荧光染色，对神经肌肉接头的染色尤为强烈。

种属反应性：

可标记大鼠、鸡和非洲爪蟾的骨骼肌。可标记大鼠和正常（但不是mdx）小鼠的心肌。还可标记鸡胗平滑肌。

Physical form

形式：纯化
液体，溶于含有0.25 mM NaCl和0.1%叠氮化钠的0.02M磷酸盐缓冲液（pH 7.6）中。

Preparation Note

以方便的等分试样在-20ºC保持长达12个月。应避免反复冻/融循环。

Legal Information

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

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wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

存储类别

12 - Non Combustible Liquids

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Andreas Schaefer et al.
Scientific reports, 9(1), 5710-5710 (2019-04-07)
Mechanical unloading (MU) by implantation of left ventricular assist devices (LVAD) has become clinical routine. This procedure has been shown to reverse cardiac pathological remodeling, with the underlying molecular mechanisms incompletely understood. Most studies thus far were performed in non-standardized
Andreas Schaefer et al.
PloS one, 11(2), e0148259-e0148259 (2016-02-04)
Previous small animal models for simulation of mechanical unloading are solely performed in healthy or infarcted hearts, not representing the pathophysiology of hypertrophic and dilated hearts emerging in heart failure patients. In this article, we present a new and economic
Payam Soltanzadeh et al.
Neuromuscular disorders : NMD, 20(8), 499-504 (2010-07-16)
Manifesting carriers of DMD gene mutations may present diagnostic challenges, particularly in the absence of a family history of dystrophinopathy. We review the clinical and genetic features in 15 manifesting carriers identified among 860 subjects within the United Dystrophinopathy Project
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全球贸易项目编号

货号GTIN
MAB164504053252467950