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Merck
모든 사진(1)

주요 문서

MABF28

Sigma-Aldrich

Anti-PAR-3 Antibody, clone 8E8

clone 8E8, from mouse

동의어(들):

Proteinase-activated receptor 3, Coagulation factor II receptor-like 2, Thrombin receptor-like 2

로그인조직 및 계약 가격 보기

크기 선택

100 μG
₩568,197

₩568,197


예상 입고일2025년 4월 17일세부사항


벌크 견적 요청

크기 선택

보기 변경
100 μG
₩568,197

About This Item

UNSPSC 코드:
12352203
eCl@ss:
32160702
NACRES:
NA.41

₩568,197


예상 입고일2025년 4월 17일세부사항


벌크 견적 요청

생물학적 소스

mouse

Quality Level

항체 형태

purified antibody

항체 생산 유형

primary antibodies

클론

8E8, monoclonal

종 반응성

mouse

종 반응성(상동성에 의해 예측)

human (based on 100% sequence homology)

기술

activity assay: suitable
flow cytometry: suitable

동형

IgG2bκ

NCBI 수납 번호

UniProt 수납 번호

배송 상태

wet ice

타겟 번역 후 변형

unmodified

유전자 정보

human ... PARD3(56288)

일반 설명

PAR-3 (also known as Coagulation factor II receptor-like 2, Thrombin receptor-like 2 or F2RL2) is an adapter protein involved in asymmetrical cell division and cell polarization processes. It seems to play a central role in the formation of epithelial tight junctions. Its association with PARD6B may prevent the interaction of PAR-3 with F11R/JAM1, thereby preventing tight junction assembly. The PARD6-PAR-3 complex links GTP bound Rho small GTPases to atypical protein kinase C proteins. PAR-3 interacts with PARD6A and PARD6B. Isoform 2, but not at least isoform 3 interacts with PRKCZ. PAR-3 interacts with PRCKI. PAR-3 forms part of a complex with PARD6A or PARD6B, PRKCI or PRKCZ and CDC42 or RAC1. PAR-3 interacts with F11R/JAM1. Antibodies against PAR-3 are present in sera from patients with cutaneous T cell lymphomas.

면역원

KLH-conjugated linear peptide corresponding to human PAR-3.

애플리케이션

Anti-PAR-3 Antibody, clone 8E8 detects level of PAR-3 & has been published & validated for use in FC, EA.
Flow Cytometry Analysis: A previous lot was used by an independent laboratory in FC. (Petrova, Y., et al. (2008). Centr Eur J Immunol. 33 (1):14-18.)

Activity Assay Analysis (platelet aggregation): A previous lot was used by an independent laboratory in platelet aggregation assay. (Petrova, Y., et al. (2008). Centr Eur J Immunol. 33 (1):14-18.)
Research Category
Infectious Diseases
Research Sub Category
Inflammation & Autoimmune Mechanisms

품질

Evaluated by Flow Cytometry in mouse platelets from washed whole blood (heparinized).

Flow Cytometry Analysis: 2 µg of this antibody detected PAR-3 in mouse platelets from washed whole blood (heparinized).

표적 설명

40 kDa calculated

결합

Replaces: MABS174

물리적 형태

Format: Purified
Protein G Purified
Purified mouse monoclonal IgG2bκ in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

저장 및 안정성

Stable for 1 year at 2-8°C from date of receipt.

분석 메모

Control
Mouse platelets from washed whole blood (heparinized)

기타 정보

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

면책조항

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


시험 성적서(COA)

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문서 라이브러리 방문

Hiroyuki Nakajima et al.
Journal of cell science, 123(Pt 4), 555-566 (2010-01-28)
Cell-shape change in epithelial structures is fundamental to animal morphogenesis. Recent studies identified myosin-II as the major generator of driving forces for cell-shape changes during morphogenesis. Lulu (Epb41l5) is a major regulator of morphogenesis, although the downstream molecular and cellular
Michael L Drummond et al.
The Journal of cell biology, 217(9), 3255-3266 (2018-06-28)
Primary cilia are polarized organelles that allow detection of extracellular signals such as Hedgehog (Hh). How the cytoskeleton supporting the cilium generates and maintains a structure that finely tunes cellular response remains unclear. Here, we find that regulation of actin
Virginia Fernández et al.
The EMBO journal, 39(21), e105479-e105479 (2020-09-29)
Structural integrity and cellular homeostasis of the embryonic stem cell niche are critical for normal tissue development. In the telencephalic neuroepithelium, this is controlled in part by cell adhesion molecules and regulators of progenitor cell lineage, but the specific orchestration
Kaviya Chinnappa et al.
Science advances, 8(2), eabj4010-eabj4010 (2022-01-13)
The evolutionary expansion and folding of the mammalian cerebral cortex resulted from amplification of progenitor cells during embryonic development. This process was reversed in the rodent lineage after splitting from primates, leading to smaller and smooth brains. Genetic mechanisms underlying

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