PROS1 (Human) Recombinant Protein (Q01)
产品名称: PROS1 (Human) Recombinant Protein (Q01)
英文名称: PROS1 (Human) Recombinant Protein (Q01)
产品编号: H00005627-Q01
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 PROS1 partial ORF ( NP_000304, 419 a.a. - 516 a.a.) recombinant protein with GST-tag at N-terminal.
 
- Sequence:
 - GLLETKVYFAGFPRKVESELIKPINPRLDGCIRSWNLMKQGASGIKEIIQEKQNKHCLVTVEKGSYYPGSGIAQFHIDYNNVSSAEGWHVNVTLNIRP
 
- Theoretical MW (kDa):
 - 36.52
 
- Preparation Method:
 - in vitro wheat germ expression system
 
- Purification:
 - Glutathione Sepharose 4 Fast Flow
 
- Storage Buffer:
 - 50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
 
- Storage Instruction:
 - Store at -80°C. Aliquot to avoid repeated freezing and thawing.
 
- Quality Control Testing:
 - 12.5% SDS-PAGE Stained with Coomassie Blue.

 
- Note:
 - Best use within three months from the date of receipt of this protein.
 
- MSDS:
 
Download
- Application Image
 
- Enzyme-linked Immunoabsorbent Assay
 
- Western Blot (Recombinant protein)
 
- Antibody Production
 
- Protein Array
 
- Entrez GeneID:
 - 5627
 
- GeneBank Accession#:
 - NM_000313
 
- Protein Accession#:
 - NP_000304
 
- Gene Name:
 - PROS1
 
- Gene Alias:
 - PROS,PS21,PS22,PS23,PS24,PS25,PSA
 
- Gene Description:
 - protein S (alpha)
 
- Omim ID:
 - 176880
 
- Gene Ontology:
 - Hyperlink
 
- Gene Summary:
 - This gene encodes a vitamin K-dependent plasma protein that functions as a cofactor for the anticoagulant protease, activated protein C (APC) to inhibit blood coagulation. It is found in plasma in both a free, functionally active form and also in an inactive form complexed with C4b-binding protein. Mutations in this gene result in autosomal dominant hereditary thrombophilia. An inactive pseudogene of this locus is located at an adjacent region on chromosome 3. [provided by RefSeq
 
- Other Designations:
 - protein S, alpha,protein Sa
 
- Gene Pathway
 
- Related Disease
 
- Abortion, Spontaneous
 - Cardiovascular Diseases
 - Carotid Stenosis
 - Chorioamnionitis
 - Coronary Disease
 - Fetal Membranes, Premature Rupture
 - Genetic Predisposition to Disease
 - Inflammation
 - Obstetric Labor, Premature
 - Pre-Eclampsia
 - Pregnancy Complications, Hematologic
 - Premature Birth
 - Protein S Deficiency
 - Stroke
 - Thrombophilia
 - Thrombosis
 - Venous Thrombosis
 
