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Thermo Fisher Scientific Phospho-Neurofibromin (Ser2741) Polyclonal Antibody
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Thermo Fisher Scientific Phospho-Neurofibromin (Ser2741) Polyclonal Antibody

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인간 Neurofibromin Ser2741 인산화 부위를 인식하는 Rabbit Polyclonal 항체로, WB 및 IHC(P)에서 사용 가능. 항원 친화 크로마토그래피로 정제된 액상 형태이며, 0.5 mg/mL 농도. 연구용으로만 사용 가능.

카탈로그번호
620-240
판매단위
pk
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마지막 업데이트 2025. 08. 01. 오후 09:34
Thermo Fisher Scientific 620-240 Phospho-Neurofibromin (Ser2741) Polyclonal Antibody 100 ug pk판매 단위 pk ·
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421,400원VAT 포함 463,540원

Thermo Fisher Scientific · Thermo Fisher Scientific Phospho-Neurofibromin (Ser2741) Polyclonal Antibody

Thermo Fisher Scientific Phospho-Neurofibromin (Ser2741) Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 0.1–1 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) 2–10 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen A synthetic peptide surrounding the epitope -PTSPY- with a phosphorylation site of Ser2741 of human neurofibromin
Conjugate Unconjugated
Form Liquid
Concentration 0.5 mg/mL
Purification Antigen affinity chromatography
Storage Buffer 25 mM Tris with proprietary stabilizer
Contains 0.01% 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)

Product Specific Information

  • Positive control: Mouse hypoxic brain

Target Information

The protein encoded by this gene is a type I integral membrane protein localized in the intermediate region between the endoplasmic reticulum and the Golgi, presumably recycling between the two compartments.
The protein is a mannose-specific lectin and is a member of a novel family of plant lectin homologs in the secretory pathway of animal cells.
Mutations in the gene are associated with a coagulation defect. Using positional cloning, the gene was identified as the disease gene leading to combined factor V-factor VIII deficiency, a rare, autosomal recessive disorder in which both coagulation factors V and VIII are diminished.

Usage Note

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

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