
Thermo Fisher Scientific NAGA Monoclonal Antibody (OTI8H7), TrueMAB
인간 NAGA 단백질을 인식하는 Mouse monoclonal 항체로 Western blot에 적합. 동결건조 형태로 제공되며, 재구성 후 약 1 mg/mL 농도 유지. PBS 완충액(8% 트레할로스) 포함, 보존제 무첨가. -20°C에서 보관, 연구용 전용.
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Applications
- Western Blot (WB): Tested dilution 1:2,000
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Mouse / IgG1 |
| Class | Monoclonal |
| Type | Antibody |
| Clone | OTI8H7 |
| Immunogen | Full length human recombinant NAGA protein produced in HEK293T cells |
| Conjugate | Unconjugated |
| Form | Lyophilized |
| Concentration | 1 mg/mL |
| Purification | Affinity chromatography |
| Storage buffer | PBS, pH 7.3, with 8% trehalose |
| Contains | No preservative |
| Storage conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping conditions | Ambient (domestic); Wet ice (international) |
Product Specific Information
For reconstitution, add 100 µL of distilled water to obtain a final antibody concentration of approximately 1 mg/mL.
For conjugation experiments, perform an additional desalting step (e.g., Zeba Spin Desalting Columns, 7K MWCO, 0.5 mL, Product #89882).
Target Information
NAGA (N-acetylgalactosaminidase, alpha), also known as alpha-galactosidase B or GALB, is a 411-amino-acid lysosomal protein belonging to the glycosyl hydrolase 27 family. It may exist as a homodimer and plays a critical role in glycolipid breakdown.
Mutations in the NAGA gene (located on chromosome 22q13.2) cause Schindler disease (types I, II, and III), also known as NAGA deficiency. The disease manifests with varying neurological severity: type I being the most severe, type III mild-to-moderate, and type II (Kanzaki disease) characterized by mild intellectual impairment and angiokeratoma corporis diffusum.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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