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Merck
모든 사진(1)

주요 문서

289R-2

Sigma-Aldrich

Myeloperoxidase (EP151) Rabbit Monoclonal Primary Antibody

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About This Item

UNSPSC 코드:
12352203
NACRES:
NA.41
가격 및 재고 정보를 현재 이용할 수 없음

생물학적 소스

rabbit

Quality Level

100
500

결합

unconjugated

항체 형태

culture supernatant

항체 생산 유형

primary antibodies

클론

EP151, monoclonal

설명

(For In Vitro Diagnostic Use in Select Regions (See Chart))

양식

buffered aqueous solution

종 반응성

human

포장

bottle of 1.0 mL predilute (289R-27)
bottle of 7.0 mL predilute (289R-28)
vial of 0.1 mL concentrate (289R-24)
vial of 0.5 mL concentrate (289R-25)
vial of 1.0 mL concentrate (289R-26)

제조업체/상표

Cell Marque®

기술

immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:100-1:500

동형

IgG

배송 상태

wet ice

저장 온도

2-8°C

유전자 정보

human ... MPO(4353)

일반 설명

Anti-myeloperoxidase detects granulocytes and monocytes in blood and precursors of granulocytes in the bone marrow. This antibody can detect myeloid cell populations of the bone marrow as well as in other sites.1-8

품질


IVD

IVD

IVD

RUO

결합

Myeloperoxidase Positive Control Slides, Product No. 289S, are available for immunohistochemistry (formalin-fixed, paraffin-embedded sections).

물리적 형태

Solution in Tris Buffer, pH 7.3-7.7, with 1% BSA and <0.1% Sodium Azide.

제조 메모

Download the IFU specific to your product lot and formatNote: This requires a keycode which can be found on your packaging or product label.

기타 정보

For Technical Service please contact: 800-665-7284 or email: [email protected]

법적 정보

Cell Marque is a registered trademark of Merck KGaA, Darmstadt, Germany

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Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 2

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

G S Pinkus et al.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 4(6), 733-741 (1991-11-01)
Immunohistochemical detection of intracellular myeloperoxidase, a major constituent of primary granules of neutrophilic myeloid cells, was determined in paraffin sections of 161 specimens using a rabbit polyclonal antibody to human myeloperoxidase and an indirect immunoperoxidase technique. In normal tissues and
J Hudock et al.
American journal of clinical pathology, 102(1), 55-60 (1994-07-01)
Paraffin sections of granulocytic sarcomas (GS) (n = 30) were immunohistochemically evaluated for CD3, CD15 (LeuM1), CD20 (L26), CD31, CD34, CD43, CD45, CD68 (KP1), lysozyme, myeloperoxidase (BM1), CD45RO (UCHL1), and LN5 with an avidin-biotin amplification system and a peroxidase-based color
Z Kaleem et al.
American journal of clinical pathology, 115(6), 876-884 (2001-06-08)
We studied immunophenotypic features of 30 cases of minimally differentiated acute myeloid leukemia (AML-M0) using multiparameter flow cytometry and immunohistochemistry and evaluated the immunophenotypic features of previously reported cases to facilitate correct identification of myeloid lineage. All but 1 of
W H Hamoudi et al.
Archives of pathology & laboratory medicine, 124(2), 315-318 (2000-02-03)
We report a case of primary acute myelomonocytic leukemia involving the bone marrow that resembled sarcomatoid carcinoma. The neoplastic cells in bone marrow biopsy specimens formed cohesive-appearing clusters and cords separated by an immature fibroblastic proliferation and myxoid stroma. Blasts
J Audouin et al.
International journal of surgical pathology, 11(4), 271-282 (2003-11-15)
Extramedullary accumulation of myeloblasts or immature myeloid cells form tumors called myeloid sarcoma in the WHO classification. Such tumors develop in lymphoid organs, bone (skull, orbit, etc.), skin, soft tissue, various mucosae and organs, and the CNS. They may precede

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