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Thermo Fisher Scientific POGK Monoclonal Antibody (OTI3D2), TrueMAB
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Thermo Fisher Scientific POGK Monoclonal Antibody (OTI3D2), TrueMAB

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POGK 단백질을 인식하는 Mouse monoclonal antibody로 Western blot과 IHC(Paraffin)에 적합. HEK293T 세포에서 발현된 full-length human recombinant POGK를 면역원으로 제작. Lyophilized 형태로 제공되며, PBS buffer(8% trehalose) 내 보관. 연구용으로만 사용 가능.

카탈로그번호
CF505670
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 05:23
Thermo Fisher Scientific CF505670 POGK Monoclonal Antibody (OTI3D2), TrueMAB 100 ug pk판매 단위 pk ·
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784,000원VAT 포함 862,400원

Thermo Fisher Scientific · Thermo Fisher Scientific POGK Monoclonal Antibody (OTI3D2), TrueMAB

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:150

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2a
Class Monoclonal
Type Antibody
Clone OTI3D2
Immunogen Full length human recombinant protein of human POGK produced in HEK293T cell
Conjugate Unconjugated
Form Lyophilized
Concentration 1 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.3, with 8% trehalose
Contains No preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Additional Formats


Product Specific Information

For reconstitution, add 100 µL of distilled water to achieve a final antibody concentration of approximately 1 mg/mL.
For conjugation experiments using this carrier-free antibody, perform an additional desalting step using Zeba Spin Desalting Columns (7K MWCO, 0.5 mL, Product #89882).


Target Information

This gene encodes a 134 kDa protein named strumpellin, predicted to have multiple transmembrane domains and a spectrin-repeat-containing domain.
It is ubiquitously expressed, with the highest expression in skeletal muscle.
The protein is associated with Strumpell disease, a form of hereditary spastic paraplegia (HSP), characterized by progressive lower extremity spasticity due to axonal degeneration in corticospinal tracts.
More than 30 loci (SPG1–33) have been implicated in hereditary spastic paraplegia.


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

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