
Thermo Fisher Scientific Lamin A/C Recombinant Superclonal Antibody (9HCLC)
Lamin A/C 단백질을 인식하는 Thermo Fisher Scientific의 Recombinant Superclonal 항체로, 인간 및 생쥐 시료에 반응합니다. Western blot에 최적화되어 있으며, 재현성 높은 결과를 제공합니다. 폴리클로날 감도와 모노클로날 특이성을 결합한 고품질 항체입니다.
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Applications
- Western Blot (WB): 1–2 µg/mL
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human, Mouse |
| Host / Isotype | Rabbit / IgG |
| Expression System | Expi293 |
| Class | Recombinant Superclonal |
| Type | Antibody |
| Clone | 9HCLC |
| Immunogen | Protein corresponding to Human LMNA (aa 400–542) |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 0.5 mg/mL |
| Purification | Protein A |
| Storage buffer | PBS, pH 7.4 |
| Contains | 0.09% 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_2633174 |
Product Specific Information
This antibody is predicted to react with Rabbit, Horse, and Pig.
Recombinant rabbit Superclonal™ antibodies are unique offerings from Thermo Fisher Scientific. They combine multiple recombinant monoclonal antibodies to provide both the sensitivity of polyclonal antibodies and the specificity of monoclonal antibodies, with the consistency of recombinant production.
These antibodies recognize multiple epitopes, enabling higher detection sensitivity for low-abundance targets. Each lot is produced with a defined mixture of light and heavy chains, ensuring reproducibility and eliminating variability found in traditional polyclonal antibodies.
Note: Formerly called “Recombinant polyclonal antibody”, now rebranded as “Recombinant Superclonal™ antibody”. The product and performance remain unchanged.
Target Information
Lamins are intermediate filament proteins forming a matrix on the inner surface of the nuclear envelope.
Lamins A and C are alternatively spliced products of the LMNA gene. Mutations in LMNA are linked to various disorders including:
- Emery-Dreifuss muscular dystrophy
- Dunnigan-type familial partial lipodystrophy (FPLD)
- Limb-girdle muscular dystrophy (LGMD1B)
- Dilated cardiomyopathy (CMD1A)
- Axonal neuropathy (Charcot-Marie-Tooth disease; CMT2B1)
- Mandibuloacral dysplasia (MAD)
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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