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high throughput screening

SignalChem’s targets out-perform the competition.
All activity assays were performed in-house under the same experimental conditions.

    HTS TARGETS IN SCREEN
 
Target Categories:     All   |  Active Kinases  |  Active Phosphatases  |  Active Phosphodiesterases  |  Cellular Proteins

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ABL1   ABL1   ABL2
ACK   ADRBK1 (GRK2)   AKT1
AKT2   AKT2   AKT3
ALK1     ALK2     ALK4  
AMPK (A1/B1/G1)   AMPK (A1/B1/G2)   AMPK (A1/B1/G3)
AMPK (A1/B2/G1)   AMPK (A2/B1/G1)   AMPK (A2/B2/G2)  
ASK1   AURORA A   AURORA A
AURORA B   AURORA C   AXL
BLK   BMX   BRAF
BRAF (V599E)   BRK   BTK
c-KIT   c-KIT(V654A)   c-MER
CAMK1   CAMK1β   CAMK1δ
CAMK1γ   CAMK1γ   CAMK2α
CAMK2β   CAMK2δ   CAMK2γ
CAMK4   CAMKK1   CAMKK2
CDK1/CyclinA1   CDK1/CyclinA2   CDK1/CyclinB1
CDK2/CyclinA1   CDK2/CyclinA2   CDK2/CyclinE1
CDK3/CyclinE1   CDK4/CyclinD1   CDK4/CyclinD3
CDK5/p25   CDK5/p29   CDK5/p35
CDK6/CyclinD1   CDK6/CyclinD3   CDK7/CyclinH/MNAT1
CDK8/CyclinC   CDK9/CyclinK   CHK1
CHK1   CHK2   CK2α1
CK2α2   CLK1   CLK2
CLK3   COT   CSK
CSK   DAPK1   DAPK2
DAPK3   DCAMKL2   DDR2
DMPK   DUSP22 (MKPX)   DYRK1α
DYRK3   EEF2K   EGFR
EIF2AK2   EIF2AK3   EPHA1
EPHA2   EPHA3   EPHA4
EPHA6   EPHB1   EPHB2
EPHB3   EPHB4   ERK1
ERK2   FAK   FER
FES   FGFR1 (FLT2)   FGFR1 (V561M)
FGFR2   FGFR3   FGFR4
FGR   FLT1   FLT3
FMS   FRK   FYN A
GCK   GRK5   GRK7
GSK3α   GSK3β   HCK
HER2   HER4   HIPK1
HIPK3   HIPK4   IGF1R
InsR   IRAK2   IRAK4
IRR   ITK   JAK3
JNK1   JNK2   JNK3
KDR   KHS1   LCK
LIMK1   LKB1/MO25a/STRADa   LOK
LRRK2   LYN A   LYN B
MAPKAPK2   MAPKAPK2   MAPKAPK3
MAPKAPK5   MARK1   MARK2
MARK3   MARK4   MEK1
MEK1 (EE)   MEK2   MEK2
MEKK2   MEKK3   MET
MET   MINK1   MLCK
MLK3   MNK1   MNK2
MRCKα   MRCKβ   MSK1
MSSK1   MST1   MST3
MST4   MUSK   MYLK2
MYLK3   MYO3β   MYT1
NEK11   NEK2   NEK3
NEK6   NEK7   NEK9
NUAK2   p38α   p38β
p38δ   p38γ   p70S6K
p70S6Kb   PAK1/CDC42   PAK2
PAK3   PAK4   PAK6
PAK7   PASK   PDE10A
PDE11A   PDE1A   PDE2A
PDE3A   PDE3B   PDE4A
PDE4B   PDE4C   PDE4D
PDE5A   PDE6B   PDE7A
PDE8A   PDE9A   PDGFRα
PDGFRα   PDGFRβ   PDK1
PHKG2   PI3K (p110α(E545K)/p85α)   PI3K (p110α/p65α)
PI3K (p110β/p85α)   PI3K (p110α/p85α)   PIM1
PIM2   PKAcα   PKAcβ
PKAcγ   PKCα   PKCα
PKCβ I   PKCβ II   PKCδ
PKCε   PKCη   PKCγ
PKCι   PKCμ   PKCν
PKCθ   PKCζ   PKD2
PKN1   PKN2/PRK2   PLK1
PLK2   PLK4   PRKG1
PTPN1 (PTP1B)   PTPN11 (SHP2)   PTPN12 (PTP-PEST)
PTPN13 (FAP-1)   PTPN2 (TC-PTP)   PTPN6 (SHP1)
PTPN7 (LC-PTP)   PTPRA (LRP)   PTPRC (CD45)
PTPRF (LAR)   PTPRS (PTPσ)   PYK2
QIK     RAF1   RAF1(EE)
RET   RIPK2   RIPK5
ROCK1   ROCK2   RON
ROR2   RSK1   RSK2
RSK3   RSK4   SGK1
SGK2   SGK3   SIK
SLK   SOK1   SPHK1  
SPHK2     SRC   SRC
SRPK1   SRPK2   STK3
STK33   SYK   TAK1-TAB1
TAOK1   TAOK2   TAOK3
TBK1   TEC   TGFβR1 Protein  
TGFβR2   TIE 2   TLK2
TOPK   TRKA   TRKB
TRKC   TSSK1   TSSK2
TTK   TXK   TYK2
TYRO3   ULK1   ULK2
WEE1   Yes1   ZAK
ZAP70    
 

The range of targets being produced span across all major signaling pathways and incorporate members of the main protein kinase and protein phosphatase target families. All of the targets utilized in SignalChem’s compound profiling service are produced in-house and our rigorous quality control measures ensure the highest specific activity and purity of our targets.



profiling services

SignalChem employs the “Gold Standard” radiolabel-based kinase screening format as part of its profiling service as it provides several advantages over some of the newer technologies. In particular, the radiolabel format provides a direct measure of catalytic activity, has the highest signal-to-noise ratio and has minimal issues with compound interference.


The discovery team at SignalChem has over 30 years of combined experience in the areas of signal transduction, enzyme kinetics and high throughput screening. We are committed to delivering the highest quality products and services and have been highly successful in establishing strong partnerships with several large life science, biotech and pharmaceutical companies.


profiling services
kinase profiling

SignalChem understands the importance of discovery timelines and works to provide the profiling results within a two-week time period. A typical report includes a detailed summary of the results, graphical and numerical representation of the findings along with the original data.

Recent References:
1. Ong, CJ. et al: Small molecule agonists of SHIP1 inhibit the phosphoinositide 3-kinase pathway in hematopoietic cells. Blood 2007 May 14; Epub.

 


    Who We Are
 

SignalChem is a life science reagent company focused on the research, development and production of innovative cell signaling products to advance basic research and drug discovery efforts, with specific emphasis on the production of highly purified biologically active human recombinant proteins

 


    NEW PRODUCTS
  ABL1, Active   Anti-DYKDDDDK Tag  
  Anti-GAPDH   Anti-GST Tag  
  Anti-HA Tag   Anti-His Tag  
  Anti-Myc Tag   Anti-V5 Tag  
  BRAF (V599E), Active   CHK1, Active  
  HIPK4, Active   IRR, Active  
  LIMK1, Unactive   MEK2, Unactive  
  TSSK2, Active    
    POPULAR PRODUCTS
  AKT1, Active   AMPK (A1/B1/G2), Active  
  AMPK (A2/B1/G1), Active   Catenin β Protein  
  ERK1, Active   FGFR1 (V561M), Active  
  GSK3 Substrate   GSK3β, Active  
  HER2, Active   MAPKAPK2, Active  
  PAK1/CDC42, Active   PDKtide  
  PLK1, Active   SRC, Active  
  STAT3 Protein   TAOK1, Active  
  TAOK2, Active        




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