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Thermo Fisher Scientific POGK Polyclonal Antibody, MaxPab
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Thermo Fisher Scientific POGK Polyclonal Antibody, MaxPab

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POGK 단백질을 인식하는 Thermo Fisher Scientific의 토끼 폴리클로날 항체. Western blot에 적합하며, 인간 시료에 반응. 친화 크로마토그래피로 정제되어 PBS 용액에 보관. 연구용으로만 사용 가능.

카탈로그번호
H00057645-D01P
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 07:13
Thermo Fisher Scientific H00057645-D01P POGK Polyclonal Antibody, MaxPab 100 ug pk판매 단위 pk ·
재고 확인 필요
582,600원VAT 포함 640,860원

Thermo Fisher Scientific · Thermo Fisher Scientific POGK Polyclonal Antibody, MaxPab

Applications

  • Western Blot (WB): 1–5 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen POGK (NP_060012.3, 1 a.a. – approximately 609 a.a.) full-length human protein
Conjugate Unconjugated
Form Liquid
Concentration See Label
Purification Affinity chromatography
Storage Buffer PBS, pH 7.4
Contains No preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

Protein sequence:
MESTAYPLNL SLKEEEEEEE IQSRELEDGP ADMQKVRICS EGGWVPALFD EVAIYFSDEE WEVLTEQQKA LYREVMRMNY ETVLSLEFPF PKPDMITRLE GEEESQNSDE WQLQGGTSAE NEESDVKPPD WPNPMNATSQ FPQPQHFDSF GLRLPRDITE LPEWSEGYPF YMAMGFPGYD LSADDIAGKF QFSRGMRRSY DAGFKLMVVE YAESTNNCQA AKQFGVLEKN VRDWRKVKPQ LQNAHAMRRA FRGPKNGRFA LVDQRVAEYV RYMQAKGDPI TREAMQLKAL EIAQEMNIPE KGFKASLGWC RRMMRRYDLS LRHKVPVPQH LPEDLTEKLV TYQRSVLALR RAHDYEVAQM GNADETPICL EVPSRVTVDN QGEKPVLVKT PGREKLKITA MLGVLADGRK LPPYIILRGT YIPPGKFPSG MEIRCHRYGW MTEDLMQDWL EVVWRRRTGA VPKQRGMLIL NGFRGHATDS VKNSMESMNT DMVIIPGGLT SQLQVLDVVV YKPLNDSVRA QYSNWLLAGN LALSPTGNAK KPPLGLFLEW VMVAWNSISS ESIVQGFKKC HISSNLEEED DVLWEIESEL PGGGEPPKDC DTESMAESN

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. Over 30 loci (SPG1–33) have been implicated in HSP.


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

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