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Thermo Fisher Scientific FANCF Polyclonal Antibody
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Thermo Fisher Scientific FANCF Polyclonal Antibody

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FANCF 단백질을 인식하는 Rabbit Polyclonal 항체로, Western blot, ELISA, IP 등에 사용 가능. 사람 및 침팬지 반응성. Affinity chromatography로 정제된 액상 항체이며, -20°C에서 보관. 연구용으로만 사용.

카탈로그번호
600-401-674
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 02:50
Thermo Fisher Scientific 600-401-674 FANCF Polyclonal Antibody 100 ug pk판매 단위 pk ·
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683,300원VAT 포함 751,630원

Thermo Fisher Scientific · Thermo Fisher Scientific FANCF Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution References
Western Blot (WB) 1:500–1:2,000 -
ELISA Assay-dependent -
Immunoprecipitation (IP) 1:1,000 -

Product Specifications

항목 내용
Species Reactivity Chimpanzee, Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide corresponding to an internal amino acid sequence of human FANCF
Conjugate Unconjugated
Form Liquid
Concentration 1.19 mg/mL
Purification Affinity chromatography
Storage Buffer 0.02M potassium phosphate, pH 7.2, with 0.15M NaCl
Contains 0.01% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

Store vial at -20°C prior to opening. Aliquot contents and freeze at -20°C or below for extended storage. Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature. This product is stable for several weeks at 4°C as an undiluted liquid. Dilute only prior to immediate use.

This antibody is directed against human FANCF protein. A BLAST analysis indicates cross-reactivity with FANCF protein from human and chimpanzee based on 100% homology with the immunizing sequence. Reactivity with homologues from other species is not known.


Target Information

The Fanconi anemia complementation group includes FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ, FANCL, FANCM, and FANCN. The previously defined group FANCH is identical to 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 this complementation group assemble into a common nuclear protein complex. The FANCF gene encodes the protein for complementation group F.


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

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