
Thermo Fisher Scientific Lamin A+C Polyclonal Antibody
Rabbit에서 생산된 Lamin A+C에 대한 Polyclonal Antibody로, Western blot 및 Flow cytometry에 적합합니다. KLH-결합 합성 펩타이드(400-450 aa, human Lamin A)를 면역원으로 사용하였으며, 핵 라미나 구조 연구 및 Lamin 관련 질환 연구에 활용 가능합니다.
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Applications and Tested Dilution
| Application | Tested Dilution | Publications |
|---|---|---|
| Western Blot (WB) | 0.5–1 µg/mL | – |
| Flow Cytometry (Flow) | 1–3 µg / 1×10⁶ cells | – |
| Miscellaneous PubMed (Misc) | – | View 5 publications |
Product Specifications
| Specification | Description |
|---|---|
| Published species | Not Applicable |
| Host / Isotype | Rabbit / IgG |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | KLH-coupled synthetic peptide within residues 400–450 of human Lamin A (Swiss Prot: P02545) |
| Conjugate | Unconjugated |
| Form | Lyophilized |
| Storage conditions | −20°C or −80°C if preferred |
| Shipping conditions | Wet ice |
Product Specific Information
Reconstitute the lyophilized powder with deionized water (or equivalent) to a final concentration of 0.5 mg/mL.
Lamins are structural protein components of the nuclear lamina, which contains three members: Lamin A, B, and C in mammalian cells. Lamin A and Lamin C are generated by alternative splicing from the same gene and share complete identity for the first 566 amino acids. Lamin A interacts with transcription factor SREBP1 via its C-terminal domain. Lamin A/C deficiency is associated with defective nuclear mechanics and impaired transcriptional activation. Lamin A/C is cleaved by caspase-6 and serves as a marker for caspase-6 activation.
This antibody (Rabbit Anti-Lamin A+C Polyclonal Antibody) is developed in rabbit using a KLH-coupled synthetic peptide within residues 400–450 of human Lamin A (Swiss Prot: P02545).
Target Information
Lamins are intermediate filament proteins that form a matrix on the inner surface of the nuclear envelope. These proteins exist in multiple cell types as three major forms (A, B, and C). Lamins A and C are alternatively spliced products of the LMNA gene.
Mutations in the LMNA gene are associated with 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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