Thermo Fisher Scientific TEIF Polyclonal Antibody
Human 및 Mouse 시료에 반응하는 Rabbit Polyclonal Antibody로, Western Blot과 Immunoprecipitation에 적합. Antigen affinity chromatography로 정제되었으며, 액상 형태로 0.20 mg/mL 농도 제공. 연구용으로만 사용 가능.
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Applications
Western Blot (WB)
- Tested Dilution: 1:2,000–1:10,000
Immunoprecipitation (IP)
- Tested Dilution: 2–5 µg/mg lysate
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human, Mouse |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Region between residue 758 and 808 of Human telomerase transcriptional elements-interacting factor |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.20 mg/mL |
| Purification | Antigen affinity chromatography |
| Storage Buffer | TBS, pH 7.0–8.0, with 0.1% BSA |
| Contains | 0.09% sodium azide |
| Storage Conditions | 4°C |
| Shipping Conditions | Wet ice |
Product Specific Information
The recommended shelf life for this product is 1 year from date of receipt.
Target Information
Chromosome 11 comprises approximately 135 million base pairs and 1,400 genes, accounting for about 4% of human genomic DNA. It is rich in gene and disease associations.
The Atm gene, located on chromosome 11, regulates cell cycle arrest and apoptosis following double-strand DNA breaks; mutations lead to ataxia-telangiectasia.
Blood disorders such as sickle cell anemia and β-thalassemia are linked to HBB gene mutations.
Mutations in the WT1 gene are associated with Wilms’ tumors, WAGR syndrome, and Denys-Drash syndrome.
Defects in chromosome 11 can also cause Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema, and Smith-Lemli-Opitz syndrome.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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