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Thermo Fisher Scientific MYOC Polyclonal Antibody
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Thermo Fisher Scientific MYOC Polyclonal Antibody

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Human MYOC 단백질을 인식하는 Rabbit Polyclonal Antibody로 Western blot 및 IHC(P) 검증 완료. 항원 친화 크로마토그래피로 정제되었으며, PBS와 글리세롤 용액 형태로 제공. MYOC 유전자 연구 및 녹내장 관련 단백질 분석에 적합.

카탈로그번호
PA555590
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 12:18
Thermo Fisher Scientific PA555590 MYOC Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific MYOC Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 0.04–0.4 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human MYOC. Recombinant protein control fragment (Product #RP-93985).
Conjugate Unconjugated
Form Liquid
Concentration 0.1 mg/mL
Purification Antigen affinity chromatography
Storage buffer PBS, pH 7.2, with 40% glycerol
Contains 0.02% sodium azide
Storage conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions Wet ice
RRID AB_2644381

Product Specific Information

Immunogen sequence:
NLLRDKSVLE EEKKRLRQEN ENLARRLESS SQEVARLRRG QCPQTRDTAR AVPPGSREVS TWNLDTLAFQ ELKSELTEVP ASRIL

Highest antigen sequence identity to the following orthologs:

  • Mouse: 79%
  • Rat: 79%

Target Information

Myocilin is an extracellular protein expressed in the eye, including the retina, trabecular meshwork, and ciliary body. Myocilin can form homomultimers in vivo and also associate with extracellular matrix components via interactions with the Hep II domain of FibroPVRL1. It interacts with myosin regulatory light chain, suggesting a role in the actomyosin system and regulation of trabecular meshwork (TM) function, which controls intraocular pressure (IOP). Dysfunction of TM can lead to elevated IOP and glaucoma development.
MYOC (also known as TIGR) maps to chromosome 1q24.3 and mutations in this gene are linked to primary open-angle glaucoma (POAG), a major cause of blindness.


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

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