TSC2 (Human) Recombinant Protein (Q01)
产品名称: TSC2 (Human) Recombinant Protein (Q01)
英文名称: TSC2 (Human) Recombinant Protein (Q01)
产品编号: H00007249-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 TSC2 partial ORF ( NP_000539, 540 a.a. - 658 a.a.) recombinant protein with GST-tag at N-terminal.
- Sequence:
- SPPPELEERDVAAYSASLEDVKTAVLGLLVILQTKLYTLPASHATRVYEMLVSHIQLHYKHSYTLPIASSIRLQAFDFLFLLRADSLHRLGLPNKDGVVRFSPYCVCDYMEPERGSEKK
- Theoretical MW (kDa):
- 38.83
- 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:
- 7249
- GeneBank Accession#:
- NM_000548
- Protein Accession#:
- NP_000539
- Gene Name:
- TSC2
- Gene Alias:
- FLJ43106,LAM,TSC4
- Gene Description:
- tuberous sclerosis 2
- Gene Ontology:
- Hyperlink
- Gene Summary:
- Mutations in this gene lead to tuberous sclerosis complex. Its gene product is believed to be a tumor suppressor and is able to stimulate specific GTPases. The protein associates with hamartin in a cytosolic complex, possibly acting as a chaperone for hamartin. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq
- Other Designations:
- tuberin
- Related Disease
- Adenocarcinoma
- Attention Deficit Disorder with Hyperactivity
- Autistic Disorder
- Colonic Neoplasms
- Cysts
- Depressive Disorder, Major
- Epilepsy
- Epilepsy
- Esophageal Neoplasms
- Genetic Predisposition to Disease
- Malformations of Cortical Development
- Mental Disorders
- NARP
- Pigmentation Disorders
- Rectal Neoplasms
- Tuberous Sclerosis
- Tuberous sclerosis
- Urinary Bladder Neoplasms