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Rabbit Anti-Cathepsin K/AF350 Conjugated antibody (bs-1611R-AF350)
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说 明 书: 100ul  
100ul/2980.00元
大包装/询价
产品编号 bs-1611R-AF350
英文名称 Anti-Cathepsin K/AF350
中文名称 AF350标记的组织蛋白酶K抗体
别    名 Cathepsin K; Procathepsin K; Cathepsin K precursor; Cathepsin O; Cathepsin O1; Cathepsin O2; Cathepsin X; CathepsinK; CTS02; CTSK; CTSK protein; CTSO; CTSO1; CTSO2; MGC23107; PKND; PYCD; Pycnodysostosis; cath-K; CK.  
规格价格 100ul/2980元 购买        大包装/询价
说 明 书 100ul  
研究领域 合成与降解  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Rat,  (predicted: Human, Mouse, Dog, Pig, Cow, Horse, Guinea Pig, )
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 36kDa
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human Cathepsin K
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 a lysosomal cysteine proteinase involved in bone remodeling and resorption. This protein, which is a member of the peptidase C1 protein family, is predominantly expressed in osteoclasts. However, the encoded protein is also expressed in a significant fraction of human breast cancers, where it could contribute to tumor invasiveness. Mutations in this gene are the cause of pycnodysostosis, an autosomal recessive disease characterized by osteosclerosis and short stature. This gene may be subject to RNA editing. [provided by RefSeq, Jul 2008].

Function:
Closely involved in osteoclastic bone resorption and may participate partially in the disorder of bone remodeling. Displays potent endoprotease activity against fibrinogen at acid pH. May play an important role in extracellular matrix degradation.

Subunit:
Belongs to the peptidase C1 family.

Subcellular Location:
Lysosome.

Tissue Specificity:
Tissue specificityPredominantly expressed in osteclasts (bones).

DISEASE:
Defects in CTSK are the cause of pycnodysostosis (PKND) [MIM:265800]. PKND is an autosomal recessive osteochondrodysplasia characterized by osteosclerosis and short stature.

Similarity:
Belongs to the peptidase C1 family.

Database links:

Entrez Gene: 1513 Human

Entrez Gene: 13038 Mouse

Entrez Gene: 29175 Rat

Omim: 601105 Human

SwissProt: P43235 Human

SwissProt: P55097 Mouse

SwissProt: O35186 Rat

Unigene: 632466 Human

Unigene: 272085 Mouse

Unigene: 5598 Rat



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

合成与降解(Synthesis and Degradation)
组织蛋白酶K(cathepsinK)是半胱氨酸蛋白酶家族的成员,它和组织蛋白酶S、L和B有很高的同源性。
在心血管方面:组织蛋白酶K参与心血管的很多病理生理过程,在动脉硬化、血管重塑与再生。也是动脉瘤生长、破裂、主动脉辩狭窄进程中主要的胶原酶之一。 在骨与关节方面:组织蛋白酶K主要位于破骨细胞,是涉及骨质再吸收的主要酶,与骨质疏松与脱钙密切相关。
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