Thermo Fisher Scientific NYX Polyclonal Antibody
인간 및 생쥐 반응성의 Rabbit Polyclonal Antibody로 Western blot과 IHC(P)에 사용 가능. 항원 친화 크로마토그래피로 정제되어 순도 95% 이상. PBS/glycerol buffer에 보관하며 장기 저장 시 -20°C에서 보존. 연구용으로만 사용.
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Applications
Western Blot (WB)
- Tested Dilution: 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC (P))
- Tested Dilution: 1:50–1:200
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human, Mouse |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | Recombinant fusion protein of human NYX |
| 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_2720219 |
Product Specific Information
The antibody was affinity-purified from rabbit antiserum by affinity chromatography using epitope-specific immunogen. The purity is >95% (by SDS-PAGE).
Target Information
The product of this gene belongs to the small leucine-rich proteoglycan (SLRP) family of proteins. Defects in this gene cause congenital stationary night blindness type 1 (CSNB1), also called X-linked congenital stationary night blindness (XLCSNB). CSNB1 is a rare inherited retinal disorder characterized by impaired scotopic vision, myopia, hyperopia, nystagmus, and reduced visual acuity. Mutations in this gene disrupt retinal interconnections involving ON-bipolar cells, leading to visual losses seen in patients with complete CSNB.
For Research Use Only.
Not for use in diagnostic procedures.
Not for resale without express authorization.
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