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Key Documents

456R-3

Sigma-Aldrich

IDH1 R132H (MRQ-67) Rabbit Monoclonal Antibody

Sinónimos:

Isocitrate dehydrogenase 1

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About This Item

Código UNSPSC:
12352203

origen biológico

rabbit

Nivel de calidad

100
500

conjugado

unconjugated

forma del anticuerpo

culture supernatant

tipo de anticuerpo

primary antibodies

clon

MRQ-67, monoclonal

descripción

For In Vitro Diagnostic Use in Select Regions

formulario

buffered aqueous solution

reactividad de especies

human

envase

vial of 0.1 mL concentrate (456R-34)
vial of 0.1 mL concentrate, Research Use Only (456R-34-RUO)
vial of 0.5 mL concentrate (456R-35)
vial of 1.0 mL concentrate (456R-36)
vial of 1.0 mL concentrate, Research Use Only (456R-36-RUO)
vial of 1.0 mL pre-dilute ready-to-use (456R-37)
vial of 1.0 mL pre-dilute, Research Use Only (456R-37-RUO)
vial of 7.0 mL pre-dilute ready-to-use (456R-38)
vial of 7.0 mL pre-dilute, ready-to-use, Research Use Only (456R-38-RUO)

fabricante / nombre comercial

Cell Marque

técnicas

immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:25-1:100 (concentrated)

isotipo

IgG

control

acute myeloid leukemia, astrocytoma, glioblastoma, oligodendroglioma

Condiciones de envío

wet ice

temp. de almacenamiento

2-8°C

visualización

cytoplasmic

Información sobre el gen

human ... IDH1(3417)

Categorías relacionadas

Descripción general

Isocitrate dehydrogenase 1 (IDH1) functions as an enzyme in the Krebs (citric acid) cycle and is biologically active in the cytoplasmic and peroxisomal compartments under normal conditions. The occurrence of heterozygous missense mutations at an arginine residue at codon 132 (R132) within the coding region for the substrate binding site of IDH1 has been described to promote oncogenesis in several malignancies. Of the identified mutant variants, a histidine substitution (R132H) is one of the more frequently observed point mutations in certain tumor groups of gliomas. Mutations involving IDH1 have been implicated as early events during gliomagenesis and IDH1 mutation status was incorporated into the 2016 WHO Classification of Tumors of the Central Nervous System as a new parameter for sub-classifying diffuse astrocytic and oligodendrogliomal tumors.3,4 Immunohistochemical identification of IDH1 R132H immunoreactivity can be used as a tool in screening tumors that may be harboring this mutation, such as low grade diffuse and anaplastic astrocytomas, oligodendrogliomas, and secondary glioblastomas.

Calidad

United States - IVD
Canada - RUO
European Union - IVD
Japan - RUO

Forma física

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

Nota de preparación

Download the IFU specific to your product lot and format
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Otras notas

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

Información legal

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

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Código de clase de almacenamiento

12 - Non Combustible Liquids

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


Certificados de análisis (COA)

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Habibe Kurt et al.
The American journal of surgical pathology, 42(5), 569-577 (2018-04-11)
Isocitrate dehydrogenase 1 (IDH1) and IDH2 mutations occur in a variety of myeloid neoplasms. Immunohistochemistry (IHC)-based direct visualization of mutant clones of hematopoietic cells can be useful for rapid diagnostic screening and for monitoring treatment response. In this study, we
Takuya Watanabe et al.
The American journal of pathology, 174(4), 1149-1153 (2009-02-28)
IDH1 encodes isocitrate dehydrogenase 1, which participates in the citric acid cycle and was recently reported to be mutated in 12% of glioblastomas. We assessed IDH1 mutations in 321 gliomas of various histological types and biological behaviors. A total of
Hui Yang et al.
Clinical cancer research : an official journal of the American Association for Cancer Research, 18(20), 5562-5571 (2012-10-17)
Genes encoding for isocitrate dehydrogenases 1 and 2, IDH1 and IDH2, are frequently mutated in multiple types of human cancer. Mutations targeting IDH1 and IDH2 result in simultaneous loss of their normal catalytic activity, the production of α-ketoglutarate (α-KG), and

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