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Thermo Fisher Scientific DNMT3A Monoclonal Antibody (64B814)
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Thermo Fisher Scientific DNMT3A Monoclonal Antibody (64B814)

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DNMT3A 단백질을 검출하기 위한 Thermo Fisher Scientific의 단클론 항체. Western blot, ICC/IF, Flow cytometry에 적합. 인간과 생쥐 시료 반응. 고순도 Protein G 정제, 1 mg/mL 농도. 연구용 전용 제품.

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마지막 업데이트 2025. 08. 05. 오후 08:10
Thermo Fisher Scientific MA191490 DNMT3A Monoclonal Antibody (64B814) 100 ug pk판매 단위 pk ·
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808,400원VAT 포함 889,240원

Thermo Fisher Scientific · Thermo Fisher Scientific DNMT3A Monoclonal Antibody (64B814)

Applications and Tested Dilution

Application Tested Dilution Notes
Western Blot (WB) 1–3 µg/mL
Immunocytochemistry (ICC/IF) 5 µg/mL
Flow Cytometry (Flow) Assay-dependent

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone 64B814
Immunogen Bacteria expressed HIS-tag recombinant mouse Dnmt3a
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein G
Storage Buffer PBS with 0.05% BSA
Contains 0.05% sodium azide
Storage Conditions Store at 4°C short term. For long-term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_1955870

Product Specific Information

MA1-91490 detects Dnmt3a from mouse samples.


Target Information

Methylation of DNA at cytosine residues plays an important role in regulation of gene expression, genomic imprinting, and is essential for mammalian development.
Hypermethylation of CpG islands in tumor suppressor genes or hypomethylation of bulk genomic DNA may be linked with development of cancer.

Three families of mammalian DNA methyltransferase genes have been identified: Dnmt1, Dnmt2, and Dnmt3.

  • Dnmt1: Constitutively expressed in proliferating cells; its inactivation causes global demethylation and embryonic lethality.
  • Dnmt2: Expressed at low levels in adult tissues; inactivation does not affect DNA methylation.
  • Dnmt3 family (Dnmt3a, Dnmt3b): Strongly expressed in ES cells; expression decreases in differentiating ES cells and is low in adult somatic tissue.
    Mutations in the Dnmt3b gene are associated with the rare autosomal recessive disorder ICF syndrome (immunodeficiency, centromeric instability, and facial anomalies).

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

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