Thermo Fisher Scientific C7orf13 Polyclonal Antibody
C7orf13 단백질을 인식하는 Thermo Fisher Scientific의 토끼 폴리클로날 항체. Western blot, IHC, ICC, ELISA 등 다양한 응용에 적합. Human 시료 반응성, Protein A 정제, 액상 형태로 -20°C 보관. 연구용으로만 사용 가능.
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Applications and Tested Dilutions
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:500–1:2,000 |
| Immunohistochemistry (Paraffin) (IHC-P) | 1:50–1:200 |
| Immunohistochemistry (Frozen) (IHC-F) | 1:100–1:500 |
| Immunocytochemistry (ICC/IF) | 1:100–1:500 |
| ELISA | 1:500–1:1,000 |
Product Specifications
| Specification | Description |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | KLH-conjugated synthetic peptide derived from human C7orf13 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Protein A |
| Storage Buffer | 0.01M TBS, pH 7.4, with 1% BSA and 50% glycerol |
| Contains | 0.02% ProClin 300 |
| Storage Conditions | -20°C |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
Target Information
Chromosome 7 is approximately 158 million bases long, encodes over 1000 genes, and represents about 5% of the human genome. It has been linked to several genetic disorders, including Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia, and Shwachman-Diamond syndrome.
Deletions in the q arm of chromosome 7 are associated with Williams-Beuren syndrome, characterized by mild intellectual disability, distinctive facial features, and sociable personality. Such deletions are also observed in myeloid disorders, including acute myelogenous leukemia and myelodysplasia.
The C7orf13 gene product has been provisionally designated as C7orf13 pending further characterization.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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