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Merck
모든 사진(1)

주요 문서

OP44

Sigma-Aldrich

Anti-APC (Ab-1) Mouse mAb (FE9)

liquid, clone FE9, Calbiochem®

동의어(들):

Anti-Adenomatous Polyposis Coli

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About This Item

UNSPSC 코드:
12352203
NACRES:
NA.43
가격 및 재고 정보를 현재 이용할 수 없음 고객지원팀으로 연락바랍니다.

생물학적 소스

mouse

Quality Level

항체 형태

purified antibody

항체 생산 유형

primary antibodies

클론

FE9, monoclonal

양식

liquid

포함

≤0.1% sodium azide as preservative

종 반응성

rat, human, mouse

제조업체/상표

Calbiochem®

저장 조건

do not freeze

동형

IgG1

배송 상태

wet ice

저장 온도

2-8°C

타겟 번역 후 변형

unmodified

유전자 정보

human ... APC(324)

일반 설명

Anti-APC (Ab-1), mouse monoclonal, clone FE9, recognizes full length APC (p300) in HCT116 cells and truncated APC (p147) in SW480 cells. It is validated for Western botting.
Protein G purified mouse monoclonal antibody generated by immunizing mice with the specified immunogen and fusing splenocytes with SP40 cells. Recognizes the ~300 kDa APC protein as well as a variety of truncated forms.
Recognizes full length APC (p300) in HCT116 cells and truncated APC (p147) in SW480 cells.
  • Antibody Target Gene Symbol: APC
  • Target Synonym: AI047805, Apc7, AU020952, AW124434, BTPS2, DP2, DP2.5, DP3, Familial adenomatous polyposis, FAP, GS, Min, RATAPC
  • Entrez Gene Name: adenomatous polyposis coli
  • Hu Entrez ID: 324 (Related Antibodies: OP80, ST1150, OP62, OP47L)
  • Mu Entrez ID: 11789
  • Rat Entrez ID: 24205
  • 면역원

    a synthetic peptide corresponding to the N-terminal 35 amino acids of APC

    애플리케이션

    Immunoblotting (1 µg/ml, see comments)

    포장

    Please refer to vial label for lot-specific concentration.

    경고

    Toxicity: Standard Handling (A)

    물리적 형태

    In 50 mM sodium phosphate buffer, pH 7.5, 0.2% gelatin.

    분석 메모

    Positive Control
    HCT116 cells for p300, SW480 cells for truncated APC (p147)

    기타 정보

    Koetsier, P. A., et al. 1993. BioTechniques15, 258.
    Smith, K. J., et al. 1993. Proc. Natl. Acad. Sci., USA90, 2846.
    Su, L.-K., et al. 1993. Can. Res.53, 2728.
    Boynton, R. F., et al. 1992. Proc. Natl. Acad. Sci. USA89, 3385.
    D′Amico, D., et al. 1992. Cancer Res.52, 1996.
    Fearon, E. R., and Jones, P. A., 1992. FASEB J.6, 2783.
    Miyoshi, Y., et al. 1992. Proc. Natl. Acad. Sci. USA89, 4452.
    Powell, S. M., et al. 1992. Nature359, 235.
    Groden, J., et al. 1991. Cell66, 589.
    Kinzler, K. W., et al. 1991. Science253, 661.
    Nishisho, I., et al. 1991. Science253, 665.

    법적 정보

    CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

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    Storage Class Code

    11 - Combustible Solids

    WGK

    WGK 1

    Flash Point (°F)

    Not applicable

    Flash Point (°C)

    Not applicable


    시험 성적서(COA)

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    문서 라이브러리 방문

    Jason L Larabee et al.
    The Journal of biological chemistry, 286(22), 19364-19372 (2011-04-14)
    The production of cAMP from Bacillus anthracis edema toxin (ET) activates gene expression in macrophages through a complex array of signaling pathways, most of which remain poorly defined. In this study, the tumor suppressor protein adenomatous polyposis coli (APC) was
    Tamar Evron et al.
    Oncogenesis, 10(9), 63-63 (2021-09-24)
    The Wnt signaling pathways play fundamental roles during both development and adult homeostasis. Aberrant activation of the canonical Wnt signal transduction pathway is involved in many diseases including cancer, and is especially implicated in the development and progression of colorectal
    Dipon Das et al.
    DNA repair, 24, 15-25 (2014-12-03)
    Colorectal cancer (CRC) patients with APC mutations do not benefit from 5-FU therapy. It was reported that APC physically interacts with POLβ and FEN1, thus blocking LP-BER via APC's DNA repair inhibitory (DRI) domain in vitro. The aim of this
    Hideaki Toki et al.
    Cancer science, 104(7), 937-944 (2013-04-05)
    Mutant mouse models are indispensable tools for clarifying the functions of genes and elucidating the underlying pathogenic mechanisms of human diseases. We carried out large-scale mutagenesis using the chemical mutagen N-ethyl-N-nitrosourea. One specific aim of our mutagenesis project was to
    Mireia Menéndez et al.
    Gastroenterology, 134(1), 56-64 (2008-01-02)
    We identified the APC N1026S variant of unknown malignant potential in the adenomatous polyposis coli (APC) gene in a Spanish attenuated familial adenomatous polyposis (AFAP) family. The variant was located in the first of the 4 highly conserved 15-amino acid

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