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Thermo Fisher Scientific NF1 Monoclonal Antibody (McNFn27a)
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Thermo Fisher Scientific NF1 Monoclonal Antibody (McNFn27a)

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NF1 단백질을 검출하는 mouse monoclonal antibody로, Human, Mouse, Rat 시료에 반응합니다. Western blot, ICC/IF, ELISA, IP 등 다양한 응용에 적합하며, Protein G로 정제된 액상형 제품입니다. 1 mg/mL 농도, PBS/BSA buffer에 보관하며 연구용으로만 사용됩니다.

카탈로그번호
MA1084
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 09:21
Thermo Fisher Scientific MA1084 NF1 Monoclonal Antibody (McNFn27a) 200 ug pk판매 단위 pk ·
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Thermo Fisher Scientific · Thermo Fisher Scientific NF1 Monoclonal Antibody (McNFn27a)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 5–10 µg/mL
Immunocytochemistry (ICC/IF) 2 µg/mL
ELISA Assay-dependent
Immunoprecipitation (IP) Assay-dependent
Affinity Purification (AP) Assay-dependent

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone McNFn27a
Immunogen Synthetic peptide corresponding to the N-terminal residues 27–41 of human neurofibromin
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein G
Storage Buffer PBS with 1 mg/mL BSA
Contains 0.05% sodium azide
Storage Conditions −20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_560294

Product Specific Information

MA1-084 detects neurofibromin in human, rat, and mouse cells.
It has been successfully used in Western blot procedures, detecting a ~230–260 kDa protein.
The immunogen is a synthetic peptide corresponding to the N-terminal residues 27–41 of human neurofibromin.


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 apparatus, presumably recycling between the two compartments.
It is a mannose-specific lectin and a member of a novel family of plant lectin homologs in the secretory pathway of animal cells.
Mutations in this gene are associated with a coagulation defect. The gene was identified as responsible for combined factor V-factor VIII deficiency, a rare autosomal recessive disorder in which both coagulation factors V and VIII are diminished.


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

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