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Merck

445R-1

Sigma-Aldrich

NKX2.2 (EP336) Rabbit Monoclonal Primary Antibody

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About This Item

Kod UNSPSC:
12352203

pochodzenie biologiczne

rabbit

Poziom jakości

100
500

białko sprzężone

unconjugated

forma przeciwciała

culture supernatant

rodzaj przeciwciała

primary antibodies

klon

EP336, monoclonal

opis

For In Vitro Diagnostic Use in Select Regions

Postać

buffered aqueous solution

reaktywność gatunkowa

human

opakowanie

vial of 0.1 mL concentrate (445R-14)
vial of 0.1 mL concentrate Research Use Only (445R-14-RUO)
vial of 0.5 mL concentrate (445R-15)
vial of 1.0 mL concentrate (445R-16)
vial of 1.0 mL concentrate Research Use Only (445R-16-RUO)
vial of 1.0 mL pre-dilute Research Use Only (445R-17-RUO)
vial of 1.0 mL pre-dilute ready-to-use (445R-17)
vial of 7.0 mL pre-dilute ready-to-use (445R-18)
vial of 7.0 mL pre-dilute ready-to-use Research Use Only (445R-18-RUO)

producent / nazwa handlowa

Cell Marque

metody

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

izotyp

IgG

kontrola

Ewing’s sarcoma, pancreas

Warunki transportu

wet ice

temp. przechowywania

2-8°C

wizualizacja

nuclear

Opis ogólny

NKX2.2 is a homeodomain transcription factor that plays a role in neuroendocrine and glial differentiation. NKX2.2 is upregulated in Ewing′s sarcoma as a result of the oncogenic EWS-FLI1 fusion protein. As one of many small round blue cell tumors, Ewing′s sarcoma can be difficult to diagnose due to the characteristic undifferentiated morphology. NKX2.2 has proven its utility as a sensitive maker for distinguishing Ewing′s sarcoma from other round blue cell tumors when used in a panel.

Jakość


IVD

IVD

IVD

RUO

Postać fizyczna

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

Uwaga dotycząca przygotowania

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Inne uwagi

For Technical Service please contact: 800-665-7284 or email: service@cellmarque.com

Informacje prawne

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

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Kod klasy składowania

12 - Non Combustible Liquids

Klasa zagrożenia wodnego (WGK)

WGK 2

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable


Certyfikaty analizy (CoA)

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Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Yoshinari Yamamoto et al.
Journal of cytology, 32(1), 30-32 (2015-05-08)
Renal Ewing sarcoma (ES) is a rare malignant tumor characterized by fusion of the EWSR1 gene with a member of the ETS family of oncogenes, arising at a specific chromosomal translocation. Diagnosis of ES can be problematic, especially from cytological
Arvind Rajwanshi et al.
Journal of cytology, 26(1), 1-10 (2009-01-01)
Malignant small round cell tumors are characterised by small, round, relatively undifferentiated cells. They generally include Ewing's sarcoma, peripheral neuroectodermal tumor, rhabdomyosarcoma, synovial sarcoma, non-Hodgkin's lymphoma, retinoblastoma, neuroblastoma, hepatoblastoma, and nephroblastoma or Wilms' tumor. Other differential diagnoses of small round
Richard Smith et al.
Cancer cell, 9(5), 405-416 (2006-05-16)
Our understanding of Ewing's sarcoma development mediated by the EWS/FLI fusion protein has been limited by a lack of knowledge regarding the tumor cell of origin. To circumvent this, we analyzed the function of EWS/FLI in Ewing's sarcoma itself. By
Yin P Hung et al.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 29(4), 370-380 (2016-02-06)
Ewing sarcoma shows considerable histologic overlap with other round cell tumors. NKX2-2, a homeodomain transcription factor involved in neuroendocrine/glial differentiation and a downstream target of EWSR1-FLI1, has been reported as an immunohistochemical marker for Ewing sarcoma. We assessed the specificity
Akihiko Yoshida et al.
The American journal of surgical pathology, 36(7), 993-999 (2012-03-27)
Ewing sarcoma is a high-grade round cell sarcoma that affects bones and soft tissues in children and young adults. Its diagnosis can be challenging, and the differential diagnoses include a wide variety of small round cell tumors. CD99 and FLI-1

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