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您当前的位置:首页 > 抗体 > SMN相关蛋白抗体

SMN相关蛋白抗体

  • 产品货号:mlR12640-1 收藏此商品
  • 销售价:1580.00-2480.00
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产品 :  mlR12640

英文名称 :  SMNDC1

中文名称 :  SMN相关蛋白抗体

    :  30 kDa splicing factor SMNrp; MGC106917; MGC112663; SMN related protein; SMN-related protein; smndc1; SMNR; SPF30; SPF30_HUMAN; Splicing factor 30, survival of motor neuron-related; Survival motor neuron domain containing 1; Survival motor neuron domain containing protein 1; Survival motor neuron domain-containing protein 1; Survival of motor neuron related splicing factor 30; Survival of motor neuron-related-splicing factor 30.  

研究领域 :  细胞生物  神经生物学  细胞凋亡  细胞周期蛋白  表观遗传学  

抗体来源 :  Rabbit

克隆类型 :  Polyclonal

交叉反应 :  Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Rabbit, Sheep,

产品应用 :  IHC-P=1:400-800 IHC-F=1:400-800 ICC=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.

:  26kDa

细胞定位 :  细胞核

    :  Lyophilized or Liquid

    :  1mg/ml

:  KLH conjugated synthetic peptide derived from human SMNDC1:131-230/238

    :  IgG

纯化方法 :  affinity purified by Protein A

:  0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.

保存条件 :  Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.

PubMed :  PubMed

产品介绍 :  This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. The protein encoded by this gene is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene. [provided by RefSeq, Jul 2008]

Function:

Necessary for spliceosome assembly. Overexpression causes apoptosis.

Subcellular Location:

Nucleus speckle. Nucleus > Cajal body. Detected in nuclear speckles containing snRNP and in Cajal (coiled) bodies.

Tissue Specificity:

Detected at intermediate levels in skeletal muscle, and at low levels in heart and pancreas.

Similarity:

Belongs to the SMN family.

Contains 1 Tudor domain.

SWISS:

O75940

Gene ID:

10285

Important Note:

This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

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