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Thermo Fisher Scientific SQSTM1 Polyclonal Antibody, MaxPab
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Thermo Fisher Scientific SQSTM1 Polyclonal Antibody, MaxPab

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Human SQSTM1 단백질을 인식하는 Rabbit Polyclonal 항체로, Western blot에 적합합니다. Affinity chromatography로 정제되었으며, PBS(pH 7.4)에 보존제가 포함되지 않은 액상 형태입니다. NF-κB 신호전달 관련 연구에 유용합니다.

카탈로그번호
H00008878-D01P
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 09:08
Thermo Fisher Scientific H00008878-D01P SQSTM1 Polyclonal Antibody, MaxPab 100 ug pk판매 단위 pk ·
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582,600원VAT 포함 640,860원

Thermo Fisher Scientific · Thermo Fisher Scientific SQSTM1 Polyclonal Antibody, MaxPab

Applications

Western Blot (WB)

  • Tested Dilution: 1–5 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen SQSTM1 (NP_003891.1, 1–440 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

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 (NF-κB) signaling pathway. The protein functions as a scaffolding/adaptor protein in concert with TNF receptor-associated factor 6 to mediate activation of NF-κB in response to upstream signals. Alternatively spliced transcript variants encoding either the same or different isoforms have been identified for this gene. Mutations in this gene result in 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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