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货号： bs-9314R-AF555 基本售价： 2980.0 元 规格： 100ul
产品信息
- 产品编号
- bs-9314R-AF555
- 英文名称
- Anti-MAP7D1/AF555
- 中文名称
- AF555标记的精氨酸/脯氨酸富含卷曲蛋白1抗体
- 别 名
- Arginine/proline rich coiled coil 1; Arginine/proline rich coiled coil domain containing protein 1; Arginine/proline-rich coiled-coil domain-containing protein 1; MA7D1_HUMAN; MAP7 domain containing 1; MAP7 domain containing protein 1; MAP7 domain-containing protein 1; MAP7D1; MGC117315; PARCC1; Proline arginine rich coiled coil 1; Proline/arginine rich coiled coil domain containing protein 1; Proline/arginine-rich coiled-coil domain-containing protein 1; RPRC1.
- 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 免疫学
- 抗体来源
- Rabbit
- 克隆类型
- Polyclonal
- 交叉反应
- Human, Mouse, Rat, Dog, Pig, Cow, Rabbit, Sheep,
- 产品应用
- IF=1:50-200
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
- 分 子 量
- 93kDa
- 性 状
- Lyophilized or Liquid
- 浓 度
- 1mg/ml
- 免 疫 原
- KLH conjugated synthetic peptide derived from human MAP7D1/RPRC1
- 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:
Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.
Subcellular Location:
Cytoplasm, cytoskeleton, spindle.
Similarity:
Belongs to the MAP7 family.
Database links:Entrez Gene: 55700 Human
SwissProt: Q3KQU3 Human
Unigene: 356096 Human
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.