Thermo Fisher Scientific EVC2 Polyclonal Antibody
EVC2 단백질을 인식하는 Thermo Fisher Scientific의 염소 유래 폴리클로날 항체. Western blot 및 IHC(P)에서 검증됨. 인간 시료에 반응하며, 뼈 형성과 골격 발달 관련 연구에 적합. 고순도 액상 형태로 안정적인 보관 가능.
- 카탈로그번호
- PA5142050
- 판매단위
- pk
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Applications
| Application | Tested Dilution |
|---|---|
| Western Blot (WB) | 0.5 µg/mL |
| Immunohistochemistry (Paraffin) (IHC (P)) | 2–4 µg/mL |
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Goat / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Peptide with sequence C-LNAKKAMRALGMD |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.5 mg/mL |
| Purification | Ammonium sulfate precipitation |
| Storage Buffer | TBS, pH 7.3, with 0.5% BSA |
| Contains | 0.02% sodium azide |
| Storage Conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping Conditions | Wet ice |
| RRID | AB_2932713 |
Product Specific Information
- Expected to recognize isoform 1 (NP_667338.3) and isoform 2 (NP_001159608.1).
- Tested in Peptide ELISA: antibody detection limit dilution 1:16,000.
Target Information
This gene encodes a protein that functions in bone formation and skeletal development.
Mutations in this gene, as well as in a neighboring gene that lies in a head-to-head configuration, cause Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia also known as chondroectodermal dysplasia.
Mutations in this gene also cause acrofacial dysostosis Weyers type (Curry-Hall syndrome), which combines limb and facial abnormalities.
Alternative splicing results in multiple transcript variants.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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