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Thermo Fisher Scientific Nucleostemin Monoclonal Antibody (2C8D5)
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Thermo Fisher Scientific Nucleostemin Monoclonal Antibody (2C8D5)

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Human 및 Mouse 시료에서 GNL3(Nucleostemin) 검출용 mouse monoclonal antibody. Western blot, FACS, ELISA에 사용 가능. Protein G 정제, 1 mg/mL 농도, PBS buffer에 0.05% sodium azide 포함. 연구용으로만 사용.

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마지막 업데이트 2025. 08. 04. 오전 07:17
Thermo Fisher Scientific MA517082 Nucleostemin Monoclonal Antibody (2C8D5) 100 ug pk판매 단위 pk ·
재고 확인 필요
661,800원VAT 포함 727,980원

Thermo Fisher Scientific · Thermo Fisher Scientific Nucleostemin Monoclonal Antibody (2C8D5)

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Flow Cytometry (Flow) 1:200–1:400
ELISA 1:10,000

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone 2C8D5
Immunogen Purified recombinant fragment of human GNL3 (amino acids 1–226) 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. Avoid freeze/thaw cycles.
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2538553

Product Specific Information

MA5-17082 targets GNL3 in FACS, indirect ELISA, and WB applications, showing reactivity with Human and Mouse samples.
The immunogen is a purified recombinant fragment of human GNL3 (amino acids 1–226) expressed in E. coli.
MA5-17082 detects GNL3, which has a predicted molecular weight of approximately 62 kDa.

Target Information

Arylsulfatase F (ARSF) is a 590 amino acid secretory protein belonging to the sulfatase family of bone and cartilage matrix proteins.
It uses calcium as a cofactor to catalyze reactions important for maintaining proper bone composition.
Unlike other family members such as Arylsulfatase E, its activity is not inhibited by warfarin.
The ARSF gene maps to human chromosome X, which contains about 153 million base pairs and over 1,000 genes.
Chromosome X, together with chromosome Y, is responsible for sex determination.
Abnormalities in sex chromosome number or combination can lead to conditions such as Turner’s syndrome, color blindness, hemophilia, and Duchenne muscular dystrophy.


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

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