CTSH (Human) Native Protein
产品名称: CTSH (Human) Native Protein
英文名称: CTSH (Human) Native Protein
产品编号: P4031
产品价格: 0
产品产地: 台湾
品牌商标: Abnova
更新时间: null
使用范围: null
亚诺法生技股份有限公司(Abnova)
- 联系人 :
- 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
- 邮编 : 11493
- 所在区域 : 台湾
- 电话 : +886-920**1152 点击查看
- 传真 : 点击查看
- 邮箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Human CTSH (P09668) native protein from human liver.
- Form:
- Liquid
- Preparation Method:
- Native protein purified from human liver
- Purity:
- ≥ 95% by SDS-PAGE
- Activity:
- 1.96 units/mg protein
- Storage Buffer:
- In 50 mM sodium acetate, 100 mM NaCl, 1 mM EDTA, pH 5.5
- Storage Instruction:
- Store at -80°C.
Aliquot to avoid repeated freezing and thawing.
- Application Image
- Functional Study
- SDS-PAGE
- Entrez GeneID:
- 1512
- Protein Accession#:
- P09668
- Gene Name:
- CTSH
- Gene Alias:
- ACC-4,ACC-5,CPSB,DKFZp686B24257,MGC1519,minichain
- Gene Description:
- cathepsin H
- Omim ID:
- 116820
- Gene Ontology:
- Hyperlink
- Gene Summary:
- The protein encoded by this gene is a lysosomal cysteine proteinase important in the overall degradation of lysosomal proteins. It is composed of a dimer of disulfide-linked heavy and light chains, both produced from a single protein precursor. The encoded protein, which belongs to the peptidase C1 protein family, can act both as an aminopeptidase and as an endopeptidase. Increased expression of this gene has been correlated with malignant progression of prostate tumors. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq
- Other Designations:
- N-benzoylarginine-beta-naphthylamide hydrolase,aleurain,cathepsin B3,cathepsin BA
- Gene Pathway
- Related Disease
- Alzheimer Disease
- Alzheimer disease
- Carcinoma
- Cardiovascular Diseases
- Celiac Disease
- Cognition
- Diabetes Mellitus, Type 1
- Diabetes Mellitus, Type 2
- Edema
- Genetic Predisposition to Disease
- Lung Neoplasms
- Prostatic Neoplasms
- Pulmonary Disease, Chronic Obstructive
- Urinary Bladder Neoplasms
- Werner syndrome