Thermo Fisher Scientific FAM13B1 Polyclonal Antibody
FAM13B1 단백질을 인식하는 Rabbit Polyclonal 항체로, WB, IHC, ICC, ELISA 등에 사용 가능합니다. Human, Mouse, Rat에 반응하며, Protein A로 정제된 1 mg/mL 액상 제품입니다. -20°C 보관, 연구용 전용입니다.
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Applications and Tested Dilutions
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:500–1:2,000 |
| Immunohistochemistry (Paraffin) (IHC-P) | Assay-dependent |
| Immunohistochemistry (Frozen) (IHC-F) | 1:100–1:500 |
| Immunocytochemistry (ICC/IF) | 1:50–1:200 |
| ELISA | 1:500–1:1,000 |
Product Specifications
| Specification | Description |
|---|---|
| Species Reactivity | Human, Mouse, Rat |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | KLH-conjugated synthetic peptide derived from human FAM13B1 (amino acids 841–915) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Protein A |
| Storage Buffer | 0.01M TBS, pH 7.4, with 1% BSA, 50% glycerol |
| Contains | 0.02% ProClin 300 |
| Storage Conditions | -20°C |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
Target Information
FAM13B is a 915 amino acid protein encoded by a gene located on human chromosome 5. This chromosome comprises approximately 181 million base pairs and encodes around 1,000 genes, representing about 6% of the human genome. It is associated with several genetic conditions, including Cockayne syndrome (ERCC8 gene), familial adenomatous polyposis (APC gene), and Treacher Collins syndrome (TCOF1 gene). Deletions in the p arm of chromosome 5 cause Cri du chat syndrome, while deletions of 5q or the entire chromosome 5 are frequently observed in therapy-related acute myelogenous leukemia and myelodysplastic syndrome.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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