Z248223
J-KEM® basic temperature controller
Model 210/T, temperature -50-200 °C
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About This Item
UNSPSC Code:
41112303
Pricing and availability is not currently available.
Recommended Products
AC/DC input
120 V / 1200 watts, 10 A (model 210 and 210/T)
220-240 V / 1200 watts, 5 A (model 310)
230 V AC
feature
thermocouple type K
for mantles upto 5 L
manufacturer/tradename
Model 210/T
temperature measuring range
-50-200 °C
accuracy: 0.1 °C (1 mL to 12 L)
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General description
With timer.
Legal Information
J-KEM is a registered trademark of J-KEM Electronics, Inc.
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Siranush Vardanyan et al.
Cancers, 12(8) (2020-08-06)
The prolonged storage of glucose as glycogen can promote the quiescence of tumor cells, whereas the accumulation of an aberrant form of glycogen without the primer protein glycogenin can induce the metabolic switch towards a glycolytic phenotype. Here, we analyzed
Y Wang et al.
Oncogenesis, 6(7), e365-e365 (2017-08-02)
Mucosa-associated lymphoma antigen 1 (MALT1) is a lymphoma oncogene that regulates signal transduction as a paracaspase and an adaptor protein. Yet, the role of MALT1 in other solid cancers such as melanoma is not well-understood. Here, we demonstrate that MALT1
Carlos A Aya-Bonilla et al.
Oncotarget, 8(40), 67355-67368 (2017-10-06)
Circulating Tumour Cells (CTCs) are promising cancer biomarkers. Several methods have been developed to isolate CTCs from blood samples. However, the isolation of melanoma CTCs is very challenging as a result of their extraordinary heterogeneity, which has hindered their biological
Aysegül Tura et al.
Investigative ophthalmology & visual science, 61(5), 12-12 (2020-05-13)
Adiponectin is an insulin-sensitizing and anticarcinogenic hormone that is encoded by a gene on chromosome 3. Here, we analyzed the expression of adiponectin and its receptor Adipor1 in primary uveal melanoma (UM) with regard to the monosomy-3 status and clinical
Kayoko Oda et al.
The journal of physiological sciences : JPS, 67(4), 497-505 (2016-09-11)
Melanoma has an extremely poor prognosis due to its rapidly progressive and highly metastatic nature. Several therapeutic drugs have recently become available, but are effective only against melanoma with specific BRAF gene mutation. Thus, there is a need to identify
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