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Thermo Fisher Scientific SQSTM1 Monoclonal Antibody (GT239)
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Thermo Fisher Scientific SQSTM1 Monoclonal Antibody (GT239)

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SQSTM1 단백질을 인식하는 GT239 단클론 항체로, Western blot과 Immunocytochemistry에 최적화되어 있습니다. 인간, 마우스, 랫트에 반응하며, Protein G로 정제된 액상 형태입니다. NF-κB 신호전달 관련 연구에 유용합니다.

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마지막 업데이트 2025. 08. 05. 오후 10:15
Thermo Fisher Scientific MA531498 SQSTM1 Monoclonal Antibody (GT239) 100 ul pk판매 단위 pk ·
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657,900원VAT 포함 723,690원

Thermo Fisher Scientific · Thermo Fisher Scientific SQSTM1 Monoclonal Antibody (GT239)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:3,000
Immunocytochemistry (ICC/IF) 1:100–1:2,000

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Mouse / IgG2a
Class Monoclonal
Type Antibody
Clone GT239
Immunogen Recombinant protein encompassing a sequence within the center region of human SQSTM1
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein G
Storage Buffer PBS
Contains No preservative
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_2787129

Product Specific Information

  • Keep as concentrated solution.
  • Positive Control: HepG2, A549, H1299, Huh-7 (untreated), Huh-7 (3 µM Thapsigargin treatment for 12 hr), Huh-7 (3 µM Thapsigargin treatment for 24 hr), HepG2 (3 µM Thapsigargin treatment for 12 hr), HepG2 (3 µM Thapsigargin treatment for 24 hr), PC-12.
  • Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.

Target Information

This gene encodes a multifunctional protein that binds ubiquitin and regulates activation of the nuclear factor kappa-B (NF-κB) signaling pathway. The protein functions as a scaffolding/adaptor protein in concert with TNF receptor-associated factor 6 to mediate activation of NF-κB in response to upstream signals. Alternatively spliced transcript variants encoding either the same or different isoforms have been identified for this gene. Mutations in this gene result in sporadic and familial Paget disease of bone.


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

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