Anti-MGLAP/GIG36/FITC Conjugated抗体
产品名称: Anti-MGLAP/GIG36/FITC Conjugated抗体
英文名称: Anti-MGLAP/GIG36/FITC
产品编号: YB--4315R-FITC
产品价格: null
产品产地: 中国/美国
品牌商标: Ybscience
更新时间: 2023-08-17T10:29:50
使用范围: 科研使用
上海钰博生物科技有限公司
- 联系人 : 陈环环
- 地址 : 上海市沪闵路6088号龙之梦大厦8楼806室
- 邮编 : 200612
- 所在区域 : 上海
- 电话 : 183****2235
- 传真 : 021-60514606
- 邮箱 : shybio@126.com
Anti-MGLAP/GIG36/FITC Conjugated抗体
产品编号 | YB-4315R-FITC |
英文名称 | Anti-MGLAP/GIG36/FITC |
中文名称 | FITC标记的细胞生长抑制基因36蛋白抗体 |
别 名 | MGP; Cell growth inhibiting gene 36 protein; Cell growth-inhibiting gene 36 protein; GAMMA-CARBOXYGLUTAMIC ACID PROTEIN, MATRIX; GIG36; Matrix Gla protein; MGLAP; MGP; MGP_HUMAN; NTI. |
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 信号转导 转录调节因子 |
抗体来源 | Rabbit |
克隆类型 | Polyclonal |
交叉反应 | Human, Mouse, Rat, |
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 | 12kDa |
性 状 | Lyophilized or Liquid |
浓 度 | 1mg/ml |
免 疫 原 | KLH conjugated synthetic peptide derived from human MGLAP/GIG36 |
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: The protein encoded by this gene is secreted and likely acts as an inhibitor of bone formation. The encoded protein is found in the organic matrix of bone and cartilage. Defects in this gene are a cause of Keutel syndrome (KS). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010] Function: Associates with the organic matrix of bone and cartilage. Thought to act as an inhibitor of bone formation. Subcellular Location: Secreted. Post-translational modifications: Requires vitamin K-dependent gamma-carboxylation for its function. DISEASE: Defects in MGP are the cause of Keutel syndrome (KS) [MIM:245150]. KS is an autosomal recessive disorder characterized by abnormal cartilage calcification, peripheral pulmonary stenosis neural hearing loss and midfacial hypoplasia. Similarity: Belongs to the osteocalcin/matrix Gla protein family. Contains 1 Gla (gamma-carboxy-glutamate) domain. Database links: Entrez Gene: 4256 Human Entrez Gene: 17313 Mouse Entrez Gene: 25333 Rat Omim: 154870 Human SwissProt: P08493 Human SwissProt: P19788 Mouse SwissProt: P08494 Rat Unigene: 365706 Human Unigene: 243085 Mouse Unigene: 2379 Rat Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications |