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Thermo Fisher Scientific NUP98 Monoclonal Antibody (3G8C7)
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Thermo Fisher Scientific NUP98 Monoclonal Antibody (3G8C7)

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NUP98 단백질을 인식하는 Mouse monoclonal antibody로 Western blot, IHC, ICC, Flow cytometry, ELISA에 사용 가능. 인간 시료에 반응하며, Protein G로 정제된 1 mg/mL 액상 형태. 4°C 단기 보관, -20°C 장기 보관 권장.

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마지막 업데이트 2025. 08. 05. 오후 09:19
Thermo Fisher Scientific MA548564 NUP98 Monoclonal Antibody (3G8C7) 100 ug pk판매 단위 pk ·
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717,500원VAT 포함 789,250원

Thermo Fisher Scientific · Thermo Fisher Scientific NUP98 Monoclonal Antibody (3G8C7)

Applications and Tested Dilutions

Application Tested Dilution Notes
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (IHC) Assay-dependent
Immunocytochemistry (ICC/IF) Assay-dependent
Flow Cytometry (Flow) Assay-dependent
ELISA 1:10,000

Product Specifications

Property Description
Species Reactivity Human
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone 3G8C7
Immunogen Purified recombinant fragment of human NUP98 (AA: 1–218) expressed in E. coli
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein G
Storage Buffer PBS
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 Wet ice
RRID AB_3090978

Target Information

Signal-mediated nuclear import and export proceed through the nuclear pore complex (NPC), which is comprised of approximately 50 unique proteins collectively known as nucleoporins. The 98 kDa nucleoporin is generated through a biogenesis pathway that involves synthesis and proteolytic cleavage of a 186 kDa precursor protein. This cleavage results in the 98 kDa nucleoporin as well as a 96 kDa nucleoporin, both of which are localized to the nucleoplasmic side of the NPC.

Rat studies show that the 98 kDa nucleoporin functions as one of several docking site nucleoporins of transport substrates. The human gene has been shown to fuse to several genes following chromosome translocations in acute myelogenous leukemia (AML) and T-cell acute lymphocytic leukemia (T-ALL). This gene is one of several genes located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and various cancers including lung, ovarian, and breast cancer. Alternative splicing of this gene results in several transcript variants; however, not all variants have been fully described.


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

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