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Thermo Fisher Scientific ST14 Polyclonal Antibody
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Thermo Fisher Scientific ST14 Polyclonal Antibody

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ST14 단백질을 표적하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody로, Human 및 Mouse 시료에 반응합니다. Western blot과 ELISA에 적합하며, 고순도 Affinity Chromatography로 정제된 액상 항체입니다. 연구용으로만 사용 가능합니다.

카탈로그번호
PA5110435
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 02:46
Thermo Fisher Scientific PA5110435 ST14 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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627,600원VAT 포함 690,360원

Thermo Fisher Scientific · Thermo Fisher Scientific ST14 Polyclonal Antibody

Thermo Fisher Scientific ST14 Polyclonal Antibody

Applications and Tested Dilution

  • Western Blot (WB): 1:500–1:2,000
  • ELISA: 1 µg/mL

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant fusion protein containing a sequence corresponding to amino acids 566–855 of human ST14 (NP_068813.1)
Conjugate Unconjugated
Form Liquid
Concentration 0.45 mg/mL
Purification Affinity Chromatography
Storage Buffer PBS, pH 7.3, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2855846

Product Specific Information

Immunogen sequence:
TCTKHTYRCL NGLCLSKGNP ECDGKEDCSD GSDEKDCDCG LRSFTRQARV VGGTDADEGE WPWQVSLHAL GQGHICGASL ISPNWLVSAA HCYIDDRGFR YSDPTQWTAF LGLHDQSQRS APGVQERRLK RIISHPFFND FTFDYDIALL ELEKPAEYSS MVRPICLPDA SHVFPAGKAI WVTGWGHTQY GGTGALILQK GEIRVINQTT CENLLPQQIT PRMMCVGFLS GGVDSCQGDS GGPLSSVEAD GRIFQAGVVS WGDGCAQRNK PGVYTRLPLF RDWIKENTGV

Target Information

SOX2 is an intronless gene encoding a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and cell fate determination. The SOX2 protein is essential for stem-cell maintenance in the central nervous system and regulates gene expression in the stomach. It lies within an intron of another gene, SOX2 overlapping transcript (SOX2OT). SOX2 may act as a transcriptional activator through protein complex formation. Mutations in SOX2 are associated with bilateral anophthalmia, optic nerve hypoplasia, and syndromic microphthalmia.

Usage Notice

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

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