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Thermo Fisher Scientific ATM Monoclonal Antibody (M361)
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Thermo Fisher Scientific ATM Monoclonal Antibody (M361)

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ATM 단백질을 검출하는 Mouse IgG2b 단일클론 항체로, WB, ICC/IF, IP에 적합합니다. 인간 시료 반응성이 있으며, Protein A로 정제된 액상 형태입니다. DNA 손상 복구 및 세포주기 조절 연구에 활용됩니다.

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마지막 업데이트 2025. 08. 02. 오전 01:25
Thermo Fisher Scientific MA547697 ATM Monoclonal Antibody (M361) 100 ul pk판매 단위 pk ·
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690,200원VAT 포함 759,220원

Thermo Fisher Scientific · Thermo Fisher Scientific ATM Monoclonal Antibody (M361)

Thermo Fisher Scientific ATM Monoclonal Antibody (M361)

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:100
Immunocytochemistry (ICC/IF) 1:250
Immunoprecipitation (IP) 1:500

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2b
Class Monoclonal
Type Antibody
Clone M361
Immunogen Clone M361 was generated from a recombinant sequence corresponding to amino acids in the C-terminal region of human ATM.
Conjugate Unconjugated
Form Liquid
Concentration 0.4 mg/mL
Purification Protein A
Storage Buffer PBS with 1 mg/mL BSA, 50% glycerol
Contains 0.05% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2942678

Product Specific Information

This antibody detects a 370 kDa protein corresponding to the molecular mass of ATM on SDS-PAGE immunoblots of human A431 and Jurkat cells.

Target Information

Ataxia-telangiectasia Mutated (ATM) is a protein belonging to the PI3/PI4 kinase family. Ataxia-telangiectasia is a rare autosomal recessive disorder characterized by progressive neurologic degeneration, immunologic deficiency, and increased risk of lymphoid cancer.

The ATM gene encodes a member of the phosphoinositide 3-kinase (PI3K) superfamily. Unlike lipid kinases, ATM phosphorylates proteins and regulates cell-cycle checkpoints via downstream targets such as p53, Mdm2, BRCA1, and SMC1.

ATM plays a critical role in repairing double-stranded DNA breaks induced by ionizing radiation and other mutagens. The C-terminal region of ATM shares homology with catalytic domains of PI3 kinases. ATM becomes autophosphorylated and activated upon exposure to ionizing radiation.

AT cells are hypersensitive to ionizing radiation, exhibit impaired DNA synthesis inhibition, and show delayed p53 induction. DNA damage activates ATM kinase, initiating a cascade of reactions that regulate cell cycle, apoptosis, and DNA damage repair. Studies have also linked ATM to apoptosis regulation via Nbs1 and Chk2 in the E2F1 pathway.

Usage Note

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

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