
Thermo Fisher Scientific GNAS Monoclonal Antibody (OTI13G5), TrueMAB
GNAS 단백질을 인식하는 Mouse IgG2a 단클론 항체로, Western blot 및 IHC(P)에서 검증됨. 인간 시료에 반응하며, 동결건조 형태로 제공. 재구성 및 결합 실험용으로 적합하며, 연구용으로만 사용 가능.
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Applications
Western Blot (WB)
- Tested Dilution: 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC (P))
- Tested Dilution: 1:2,000
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Mouse / IgG2a |
| Class | Monoclonal |
| Type | Antibody |
| Clone | OTI13G5 |
| Immunogen | Full length human recombinant protein of human GNAS produced in HEK293T Cell |
| 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 distilled water to obtain a final antibody concentration of approximately 1 mg/mL.
For conjugation experiments using this carrier-free antibody, perform an additional desalting step (Zeba Spin Desalting Columns, 7K MWCO, 0.5 mL, Product #89882).
Target Information
Mutations in the GNAS gene are associated with several disorders, including:
- Pseudohypoparathyroidism types 1a and 1b
- Albright hereditary osteodystrophy
- Pseudopseudohypoparathyroidism
- McCune-Albright syndrome
- Progressive osseous heteroplasia
- Polyostotic fibrous dysplasia
- Certain pituitary tumors
The GNAS gene has a complex imprinted expression pattern, encoding multiple alternatively spliced transcripts with distinct 5′ exons located within differentially methylated regions. Some transcripts show unusual promoter proximity (14 kb apart), and one variant introduces a frameshift resulting in a structurally unrelated isoform. An antisense transcript may regulate imprinting in this region. Mutations lead to pseudohypoparathyroidism type 1a (PHP1a), which exhibits atypical autosomal dominant inheritance requiring maternal transmission for full penetrance.
For Research Use Only.
Not for use in diagnostic procedures.
Not for resale without express authorization.
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