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NTCF22---ABB brandnew in stock

Product Details

Product Details

Product Description

Product Description
Product details
Delivery time1-2 daysEstimated Lead Time3-4 weeks
Factory warraty12 monthsModule numberNTCF22
ManufacturerABBProduct Name33
Voltage range (VDC)120VDCOutput range (mA)12
Over-range protection (VDC)3.65Input range (mA)2.2
Working temperature1080System memory (Mb)11
Interface4
Color codeGreen
Weight (KG)2.5Shipping weight (KG)3.5
Dimension (mm*mm*mm)20*50*50PurposePetrochemical industries
Operation modeDirect on-boardProduct situationStop production

Our store has many brands: the following four major system spare parts are examples.
Spare parts of PLC programmable control system:
Allen-bradley:1756 1771 1785
Siemens: 6ES7 6ES5
Schneider:140CPU
GE:IC697 IC698
Motorola:MVME162 MVME137 MVME147
Xycom:XVME
Spare parts of DCS control system:
DCS distributed control system:
Invensys Foxoboro:FBM01 FBM02 FBM09 FBM10 FBM201 FBM209
Invensys Triconex: 3503E 3664 3721 3625 4351D 3700A
ABB bailey:BRC300 BRC400 BRC410 AC800 IMASI23
Westinghouse Ovation:IC31
Spare parts of servo control system:
Kollmorgen: SM71K 6SM27 AKV23F 60WKS 65WKS
Seimens: 6DD1606 6SN1118 6FC5203 6RB2000 6SC6508 6FX2007 6FM2805 6AV6542
Bosh Rexroth: HCS02.1E HMS01.1N HLB01.1C MSK060B MKE118B MSM020B MHD071B
SEW: MDX61B0022 MDS60A0040 MDF60A0015 MDV60A0015 MCH42A0220 MCV40A0075
Spare parts of robot control system:
KUKA:KRC1 KRC2 KRC4 KPS600 KCP2
ABB:3HAB 3HAA 3HAC DSQC345
FANUC:A02B A03B A04B A05B A06B
Yaskawa:CACR JUSP JZNC JANCD HW
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Direct activation of the human phospholipase C-γ isozymes (PLC-γ1, -γ2) by tyrosine phosphorylation is fundamental to the control of diverse biological processes, including chemotaxis, platelet aggregation, and adaptive immunity. In turn, aberrant activation of PLC-γ1 and PLC-γ2 is implicated in inflammation, autoimmunity, and cancer. Although structures of isolated domains from PLC-γ isozymes are available, these structures are insufficient to define how release of basal autoinhibition is coupled to phosphorylation-dependent enzyme activation. Here, we describe the first high-resolution structure of a full-length PLC-γ isozyme and use it to underpin a detailed model of their membrane-dependent regulation. Notably, an interlinked set of regulatory domains integrates basal autoinhibition, tyrosine kinase engagement, and additional scaffolding functions with the phosphorylation-dependent, allosteric control of phospholipase activation. The model also explains why mutant forms of the PLC-γ isozymes found in several cancers have a wide spectrum of activities, and highlights how these activities are tuned during disease.

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