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ELK Biotechnology Lamin A/C (phospho Ser22) rabbit pAb
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ELK Biotechnology Lamin A/C (phospho Ser22) rabbit pAb

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Lamin A/C 단백질의 Ser22 인산화 부위를 인식하는 토끼 폴리클로날 항체로, WB, IHC, IF, ELISA에 적합합니다. 핵막 및 라미나 단백질 연구에 유용하며, 인간, 마우스, 랫트에 반응합니다. -20°C에서 1년 보관 가능합니다.

판매단위
pk
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ELK Biotechnology ES6124-100UL Lamin A/C (phospho Ser22) rabbit pAb, 100UL pk판매 단위 pk ·
재고 확인 필요
402,000원VAT 포함 442,200원
ELK Biotechnology ES6124-50UL Lamin A/C (phospho Ser22) rabbit pAb, 50UL pk판매 단위 pk ·
재고 확인 필요
301,000원VAT 포함 331,100원

ELK Biotechnology · ELK Biotechnology Lamin A/C (phospho Ser22) rabbit pAb

Lamin A/C (phospho Ser22) rabbit pAb

제품 정보

항목 내용
Product name Lamin A/C (phospho Ser22) rabbit pAb
Alternative Names LMNA; LMN1; Prelamin-A/C
Applications WB; IHC; IF; ELISA
Recommended Dilutions WB: 1/500–1/2000
IHC: 1/100–1/300
ELISA: 1/5000
Other applications not yet tested
Immunogen Synthesized peptide derived from human Lamin A around the phosphorylation site of Ser22 (AA range: 2–51)
Host Rabbit
Storage -20°C / 1 year
Clonality Polyclonal
Isotype IgG
Concentration 1 mg/ml
Observed Band 74 kDa
GeneID (Human) 4000
Human Swiss-Prot No P02545
Species Reactivity Human; Mouse; Rat

세포 내 위치 (Cellular Localization)

Nucleus, nuclear envelope, nuclear lamina, nucleoplasm, and nucleus matrix.
Farnesylation of prelamin-A/C facilitates nuclear envelope targeting and subsequent cleavage by ZMPSTE24/FACE1 to remove the farnesyl group, producing mature lamin-A/C that integrates into the nuclear lamina.
EMD is required for proper localization of non-farnesylated prelamin-A/C.
[Isoform C]: Nucleus speckle.

Background

Lamin A/C (LMNA) is a structural component of the nuclear lamina, forming a two-dimensional matrix adjacent to the inner nuclear membrane. Lamin proteins are evolutionarily conserved and play essential roles in nuclear stability, chromatin organization, and gene expression. During mitosis, lamin proteins are phosphorylated, leading to reversible disassembly of the lamina.
Vertebrate lamins are classified into A and B types, and alternative splicing produces multiple transcript variants.
Mutations in LMNA are associated with several diseases, including Emery-Dreifuss muscular dystrophy, familial partial lipodystrophy, limb-girdle muscular dystrophy, dilated cardiomyopathy, Charcot-Marie-Tooth disease, and Hutchinson-Gilford progeria syndrome.
(RefSeq, Apr 2012)

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