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Thermo Fisher Scientific FANCL Polyclonal Antibody
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Thermo Fisher Scientific FANCL Polyclonal Antibody

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인간 FANCL 단백질을 인식하는 Rabbit Polyclonal 항체입니다. IHC(P)에서 1:200–1:500 희석으로 사용 가능합니다. 항원 친화 크로마토그래피로 정제되었으며, PBS와 글리세롤 완충액에 보관됩니다. 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 08. 05. 오전 08:58
Thermo Fisher Scientific PA557769 FANCL Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific FANCL Polyclonal Antibody

Applications

Tested Applications and Dilution

  • Immunohistochemistry (Paraffin) (IHC (P)): 1:200–1:500

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human FANCL. Recombinant protein control fragment (Product #RP-96016)
Conjugate Unconjugated
Form Liquid
Concentration 0.05 mg/mL
Purification Antigen affinity chromatography
Storage buffer PBS, pH 7.2, with 40% glycerol
Contains 0.02% 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_2641500

Product Specific Information

Immunogen sequence:
FPARAILEKS DFTMDCGICY AYQLDGTIPD QVCDNSQCGQ PFHQICLYEW LRGLLTSRQS FNIIFGECPY CSKPIT

Sequence identity to orthologs:

  • Mouse: 82%
  • Rat: 80%

Target Information

The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM, and FANCN (also called PALB2).
The previously defined group FANCH is the same as FANCA.

Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair.
The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex.
This gene encodes the protein for complementation group L. Alternative splicing results in two transcript variants encoding different isoforms.


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

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