Thermo Fisher Scientific EMID2 Polyclonal Antibody
EMID2 단백질을 인식하는 Rabbit Polyclonal 항체로, WB, IHC, ICC, ELISA 등 다양한 응용에 사용 가능. Human, Mouse, Rat 반응성. Protein A 정제, 1 mg/mL 농도, TBS/BSA/glycerol buffer 보존. 연구용으로 적합.
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Applications and Tested Dilutions
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 1:300 |
| Immunohistochemistry (Paraffin) (IHC-P) | 1:200–1:400 |
| Immunohistochemistry (Frozen) (IHC-F) | 1:100–1:500 |
| Immunocytochemistry / Immunofluorescence (ICC/IF) | 1:100–1:500 |
| ELISA | 1:500–1:1,000 |
Product Specifications
| Specification | Detail |
|---|---|
| Species Reactivity | Human, Mouse, Rat |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | KLH-conjugated synthetic peptide derived from human EMID2 (amino acids 65–165) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 1 mg/mL |
| Purification | Protein A |
| Storage Buffer | TBS, pH 7.4, with 1% BSA, 50% glycerol |
| Contains | 0.03% ProClin 300 |
| Storage Conditions | -20°C |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
Target Information
COL26A1 (EMID2) is a 441 amino acid protein encoded by a gene located on human chromosome 7.
Chromosome 7 spans approximately 158 million bases, contains over 1,000 genes, and accounts for about 5% of the human genome.
It has been linked to several genetic disorders, including:
- Osteogenesis imperfecta
- Pendred syndrome
- Lissencephaly
- Citrullinemia
- 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 an unusually friendly demeanor. Similar deletions are also observed in various myeloid disorders, including acute myelogenous leukemia and myelodysplasia.
For Research Use Only.
Not for use in diagnostic procedures.
Not for resale without express authorization.
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