Thermo Fisher Scientific FKSG2 Polyclonal Antibody
Thermo Fisher Scientific의 FKSG2 Polyclonal Antibody는 Human, Mouse, Rat 시료에 반응하며 Western blot에 적합합니다. 항원 친화 크로마토그래피로 정제된 고순도 항체로, 장기 보관 시 -20°C에서 안정적입니다. 연구용으로만 사용 가능합니다.
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Applications
- Western Blot (WB): 1:500–1:1,000
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human, Mouse, Rat |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Synthetic peptide corresponding to residues in Human FKSG2 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Antigen affinity chromatography |
| Storage Buffer | PBS, pH 7.2, with 50% glycerol |
| Contains | 0.02% sodium azide |
| Storage Conditions | Store at 4°C short term. For long-term storage, store at -20°C, avoiding freeze/thaw cycles. |
| Shipping Conditions | Wet ice |
| RRID | AB_2719324 |
Product Specific Information
The antibody was affinity-purified from rabbit antiserum by affinity chromatography using an epitope-specific immunogen. The purity is greater than 95% as determined by SDS-PAGE.
Target Information
Chromosome 8, composed of approximately 146 million bases, encodes about 800 genes. Translocations involving chromosome 8 and amplification of the c-Myc gene are observed in certain leukemias and lymphomas, often associated with poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8 (Warkany syndrome 2) typically results in early miscarriage but can appear in mosaic form, causing developmental and facial abnormalities. The WRN gene on chromosome 8 encodes a DNA helicase defective in Werner syndrome, an early aging disorder. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism, and Waardenburg syndrome. The FKSG2 gene product has been provisionally designated FKSG2 pending further characterization.
For Research Use Only.
Not for use in diagnostic procedures.
Not for resale without express authorization.
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