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Thermo Fisher Scientific Lamin A/C Recombinant Rabbit Monoclonal Antibody (4L8Q0)
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Thermo Fisher Scientific Lamin A/C Recombinant Rabbit Monoclonal Antibody (4L8Q0)

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Lamin A/C 단백질을 인식하는 재조합 토끼 단일클론 항체로, Western blot, IHC, ICC, ELISA, IP 등 다양한 응용에 적합합니다. 인간, 마우스, 랫트 반응성을 가지며 고순도 친화 크로마토그래피로 정제되었습니다. 연구용으로만 사용 가능합니다.

카탈로그번호
MA535284
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 03:30
Thermo Fisher Scientific MA535284 Lamin A/C Recombinant Rabbit Monoclonal Antibody (4L8Q0) 100 ul pk판매 단위 pk ·
재고 확인 필요
595,300원VAT 포함 654,830원

Thermo Fisher Scientific · Thermo Fisher Scientific Lamin A/C Recombinant Rabbit Monoclonal Antibody (4L8Q0)

Applications and Tested Dilutions

Application Tested Dilution Publications
Western Blot (WB) 1:50,000–1:300,000 View 2 publications
Immunohistochemistry (Paraffin) (IHC (P)) 1:1,000–1:4,000 -
Immunocytochemistry (ICC/IF) 1:100–1:800 -
ELISA 1 µg/mL -
Immunoprecipitation (IP) 0.5–4 µg antibody for 200–400 µg extracts -

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Published Species Human
Host / Isotype Rabbit / IgG
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone 4L8Q0
Immunogen Recombinant fusion protein containing a sequence corresponding to amino acids 403–572 of human Lamin A/C (NP_733821.1)
Conjugate Unconjugated
Form Liquid
Concentration 0.24 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.3, with 50% glycerol, 0.05% BSA
Contains 0.05% ProClin 300
Storage Conditions -20°C, avoid freeze/thaw cycles
Shipping Conditions Wet ice
RRID AB_2849186

Product Specific Information

Immunogen sequence:
SSHSSQTQGG GSVTKKRKLE STESRSSFSQ HARTSGRVAV EEVDEEGKFV RLRNKSNEDQ SMGNWQIKRQ NGDDPLLTYR FPPKFTLKAG QVVTIWAAGA GATHSPPTDL VWKAQNTWGC GNSLRTALIN STGEEVAMRK LVRSVTVVED DEDEDGDDLL HHHHGSHCSS


Target Information

Lamins are intermediate filament proteins forming a matrix on the inner surface of the nuclear envelope. They exist in three forms (A, B, and C) and are expressed in various cell types. Lamins A and C are alternatively spliced products of the LMNA gene.
Mutations in LMNA are associated with several disorders including:

  • Emery-Dreifuss muscular dystrophy
  • Dunnigan-type familial partial lipodystrophy (FPLD)
  • Limb-girdle muscular dystrophy (LGMD1B)
  • Dilated cardiomyopathy (CMD1A)
  • Axonal neuropathy (CMT2B1)
  • Mandibuloacral dysplasia (MAD)

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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