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Thermo Fisher Scientific TREX1 Polyclonal Antibody
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Thermo Fisher Scientific TREX1 Polyclonal Antibody

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Human 및 Mouse 반응성을 가진 Rabbit Polyclonal TREX1 항체로 Western Blot과 Immunocytochemistry에 적합. 항원 친화 크로마토그래피로 정제되어 순도 95% 이상. DNA 손상 반응 및 ATR 신호전달 연구용. 연구용으로만 사용 가능.

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마지막 업데이트 2025. 08. 04. 오후 06:41
Thermo Fisher Scientific PA577022 TREX1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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731,200원VAT 포함 804,320원

Thermo Fisher Scientific · Thermo Fisher Scientific TREX1 Polyclonal Antibody

Applications

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunocytochemistry (ICC/IF) 1:50–1:200

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant full length Human TREX1
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 50% 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_2720749

Product Specific Information

The antibody was affinity-purified from rabbit antiserum by affinity chromatography using epitope-specific immunogen. The purity is greater than 95% as determined by SDS-PAGE.

Target Information

Trex1 (ATRIP) is the major human 3′ to 5′ exonuclease required for checkpoint signaling after DNA damage. It is ubiquitously expressed and binds to single-stranded DNA coated with replication protein A at sites of DNA damage. It recruits the ATR checkpoint kinase to sites of DNA damage and replication stress and is required for ATR expression.
This gene uses two different open reading frames:

  • The upstream ORF encodes proteins that interact with ATR and localize to intranuclear foci induced by DNA damage, functioning as essential components of the DNA damage checkpoint.
  • The downstream ORF encodes proteins with 3′ to 5′ exonuclease activity and may be a subunit of human DNA polymerase III.

Multiple transcript variants encoding different isoforms have been identified. Mutations in this gene are associated with Aicardi-Goutières syndrome, chilblain lupus, and Cree encephalitis.


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

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