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Thermo Fisher Scientific SQSTM1 Monoclonal Antibody (2C11)
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Thermo Fisher Scientific SQSTM1 Monoclonal Antibody (2C11)

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Human 및 Mouse에서 반응하는 SQSTM1 단클론 항체로 Western blot, ICC/IF, ELISA에 적합합니다. GST 태그가 포함된 full-length recombinant protein을 면역원으로 사용하였으며, 보존제가 없는 PBS buffer에 액상 형태로 제공됩니다. 연구용으로만 사용 가능합니다.

카탈로그번호
H00008878-M01
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 03:10
Thermo Fisher Scientific H00008878-M01 SQSTM1 Monoclonal Antibody (2C11) 100 ug pk판매 단위 pk ·
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Thermo Fisher Scientific · Thermo Fisher Scientific SQSTM1 Monoclonal Antibody (2C11)

Applications

Application Tested Dilution
Western Blot (WB) 1–5 µg/mL
Immunocytochemistry (ICC/IF) 10 µg/mL
ELISA 0.03 ng/mL

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Host / Isotype Mouse / IgG2a, kappa
Class Monoclonal
Type Antibody
Clone 2C11
Immunogen SQSTM1 (AAH03139.1, 1–440 a.a) full-length recombinant protein with GST tag (MW of GST tag: 26 kDa)
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

Sequence of this protein is as follows:
MASLTVKAYL LGKEDAAREI RRFSFCCSPE PEAEAEAAAG PGPCERLLSR VAALFPALRP GGFQAHYRDE DGDLVAFSSD EELTMAMSYV KDDIFRIYIK EKKECRRDHR PPCAQEAPRN MVHPNVICDG CNGPVVGTRY KCSVCPDYDL CSVCEGKGLH RGHTKLAFPS PFGHLSEGFS HSRWLRKVKH GHFGWPGWEM GPPGNWSPRP PRAGEARPGP TAESASGPSE DPSVNFLKNV GESVAAALSP LGIEVDIDVE HGGKRSRLTP VSPESSSTEE KSSSQPSSCC SDPSKPGGNV EGATQSLAEQ MRKIALESEG RPEEQMESDN CSGGDDDWTH LSSKEVDPST GELQSLQMPE SEGPSSLDPS QEGPTGLKEA ALYPHLPPEA DPRLIESLSQ MLSMGFSDEG GWLTRLLQTK NYDIGAALDT IQYSKHPPPL

Target Information

This gene encodes a multifunctional protein that binds ubiquitin and regulates activation of the nuclear factor kappa-B signaling pathway. The protein acts as a scaffolding/adaptor with TNF receptor-associated factor 6 to mediate NF-kB activation. Alternatively spliced transcript variants encoding different isoforms have been identified. Mutations in this gene are associated with sporadic and familial Paget disease of bone.

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

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