FITC标记的突触生长相关蛋白抗体

¥2980
LMAI Bio
中国/美国/欧洲
2022-03-24 21:50

上海联迈生物工程有限公司

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上海联迈生物工程有限公司
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产品属性
供应商上海联迈生物工程有限公司
数量大量
靶点详见说明书
级别1
目录编号LM-11916R-FITC
克隆性多克隆
抗原来源Rabbit
保质期1年
抗体英文名Anti-Neugrin/FITC
抗体名Anti-Neugrin/FITC
标记物FITC标记
宿主Human, Mouse, Rat, Dog, Cow, Horse, Rabbit, Sheep,
适应物种Human, Mouse, Rat, Dog, Cow, Horse, Rabbit, Sheep,
免疫原详见说明书
亚型IGg
形态粉末、液体、冻干粉
应用范围ICC=1:50-200 IF=1:50-200
浓度1mg/ml
保存条件-20 °C
规格100ul
产品说明
FITC标记的突触生长相关蛋白抗体
英文名称Anti-Neugrin/FITC
中文名称FITC标记的突触生长相关蛋白抗体
别 名DSC92; FI58Gm; Mesenchymal stem cell protein DSC92; Neugrin; Neugrin neurite outgrowth associated; Neurite outgrowth associated protein; Neurite outgrowth-associated protein; Ngrn; NGRN_HUMAN; Spinal cord-derived protein FI58G.
规格价格100ul/2980元 购买 大包装/询价
说 明 书100ul
研究领域细胞生物 神经生物学
抗体来源Rabbit
克隆类型Polyclonal
交叉反应Human, Mouse, Rat, Dog, Cow, Horse, Rabbit, Sheep,
产品应用ICC=1:50-200 IF=1:50-200
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量31kDa
性 状Lyophilized or Liquid
浓 度1mg/ml
免 疫 原KLH conjugated synthetic peptide derived from human Neugrin
亚 型IgG
纯化方法affinity purified by Protein A
储 存 液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.
产品介绍background:
Neugrin, also known as NGRN, mesenchymal stem cell protein DSC92, neurite outgrowth-associated protein or spinal cord-derived protein FI58G, is a 291 amino acid protein that plays a role in neuronal differentiation and belongs to the neugrin family. As both a secreted and nuclear protein, neugrin exists as two alternatively spliced isoforms and is highly expressed in skeletal muscle, brain and heart. Neugrin is upregulated in neuroblastostoma cells by retinoic acid treatment and is encoded by a gene that maps to human chromosome 15q26.1. Chromosome 15 houses over 700 genes and comprises nearly 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.

Function:
May be involved in neuronal differentiation.

Subcellular Location:
Nucleus. Secreted.

Tissue Specificity:
Expressed at high levels in heart, brain and skeletal muscle. In brain, mainly expressed in neurons rather than glial cells.

Similarity:
Belongs to the neugrin family.

Database links:
UniProtKB/Swiss-Prot: Q9NPE2.2

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