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Thermo Fisher Scientific SGOL1 Polyclonal Antibody
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Thermo Fisher Scientific SGOL1 Polyclonal Antibody

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SGOL1 단백질을 인식하는 Rabbit Polyclonal 항체로, Western blot에 적합합니다. 인간 단백질에 100% 반응하며, 합성 펩타이드(C-terminal, aa 395-444)를 면역원으로 사용했습니다. 액상 형태, 0.5 mg/mL 농도, PBS(2% sucrose) 완충액에 보관됩니다.

카탈로그번호
PA545207
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 01:14
Thermo Fisher Scientific PA545207 SGOL1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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630,500원VAT 포함 693,550원

Thermo Fisher Scientific · Thermo Fisher Scientific SGOL1 Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 1 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide directed towards the C-terminal of human SGOL1 (aa 395–444)
Conjugate Unconjugated
Form Liquid
Concentration 0.5 mg/mL
Purification Affinity Chromatography
Storage Buffer PBS with 2% sucrose
Contains 0.09% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2607522

Product Specific Information

  • Peptide sequence:
    NSDRPVTRPL AKRALKYTDE KETEGSKPTK TPTTTPPETQ QSPHLSLKDI
  • Sequence homology:
    Horse: 91%
    Human: 100%
    Rat: 79%

Target Information

The protein encoded by this gene is a member of the shugoshin family of proteins. It protects centromeric cohesin from cleavage during mitotic prophase by preventing phosphorylation of a cohesin subunit. Reduced expression of this gene leads to premature loss of centromeric cohesion, mis-segregation of sister chromatids, and mitotic arrest.
Evidence suggests that this protein also protects a subset of cohesin found along chromosome arms during mitotic prophase.
An isoform lacking exon 6 plays a role in centriole cohesion.
Mutations in this gene are associated with Chronic Atrial and Intestinal Dysrhythmia (CAID) syndrome, characterized by Sick Sinus Syndrome (SSS) and Chronic Intestinal Pseudo-obstruction (CIPO).
Fibroblast cells from CAID patients show increased proliferation and senescence.
Pseudogenes of this gene exist on chromosomes 1 and 7.
Alternative splicing results in multiple transcript variants.


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

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