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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  |  Active Histone Deacetylases

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ABL1 (h)   ABL1 (m)   ABL2
ACK   ACVR2A   ACVR2B
AKT1   AKT2 (GST)   AKT2 (His)
AKT3   ALK1   ALK2
ALK3 (BMPR1A)   ALK4   ALK6 (BMPR1B)
ALK7   AMPK (A1/B1/G1)   AMPK (A1/B1/G2)
AMPK (A1/B1/G3)   AMPK (A1/B2/G1)   AMPK (A2/B1/G1)
AMPK (A2/B2/G1)   AMPK (A2/B2/G2)   AMPK (A2/B2/G3)
ASK1   AURORA A (h)   AURORA A (m)
AURORA B   AURORA C   AXL
BLK   BMPR2   BMX
BRAF   BRAF (V599E)   BRK
BRSK1     BTK   c-KIT
c-KIT (D820E)   c-KIT (N822K)   c-KIT (T670E)  
c-KIT (T670I)     c-KIT (V654A)   c-KIT (V823D)  
c-MER   CAMK1   CAMK1 beta
CAMK1 delta   CAMK1 gamma (1-330)   CAMK1 gamma (Full)
CAMK2 alpha   CAMK2 beta   CAMK2 delta
CAMK2 gamma   CAMK4   CAMKK1
CAMKK2   CDC25A   CDC25B
CDC25C   CDC7/DBF4   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/Cyclin H1/MNAT1   CDK8/CyclinC
CDK9/CyclinK   CHK1 (GST)   CHK1 (His)
CHK2   CK1 alpha1   CK1 delta
CK1 epsilon   CK1 gamma 1     CK1 gamma 2
CK1 gamma 3   CK2 alpha 1   CK2 alpha 2
CLK1   CLK2   CLK3
COT   CSK (GST)   CSK (untag)
DAPK1   DAPK2   DAPK3
DCAMKL1   DCAMKL2   DDR1
DDR2   DMPK   DUSP22 (MKPX)
DYRK1 alpha   DYRK2   DYRK3
DYRK4   EEF2K   EGFR
EIF2AK1 (HRI)   EIF2AK2   EIF2AK3
EIF2AK4   EPHA1 (h)   EPHA1 (m)
EPHA2   EPHA3   EPHA4
EPHA6   EPHA7   EPHB1
EPHB2   EPHB3   EPHB4 (GST)
EPHB4 (His)   ERK1 (GST)   ERK1 (untag)
ERK2   ERK5   FAK (393-698)
FAK (Full)   FER   FES
FGFR1 (FLT2)   FGFR1 (V561M)   FGFR2
FGFR3   FGFR3 (K650E)   FGFR4
FGR   FLT (D835Y)     FLT1
FLT3   FLT4   FMS
FRK   FYN A   GCK
GRK1   GRK2   GRK5
GRK6   GRK7   GSK3 alpha
GSK3 beta (GST)   GSK3 beta (His)   Haspin (GSG2)
HCK   HDAC1   HDAC10
HDAC11   HDAC2   HDAC3
HDAC4   HDAC5   HDAC6
HDAC7   HDAC8   HDAC9
HER2   HER4   HGK
HIPK1   HIPK2     HIPK3
HIPK4   HPK1   ICK
IGF1R   IKK alpha   IKK beta
IKKe   InsR   IRAK2
IRAK4   IRR   ITK
JAK2*     JAK3   JNK1
KDR   KHS1   LATS1
LATS2   LCK   LIMK1
LKB1/MO25a/STRADa   LOK   LRRK2
LYN A   LYN B   MAPKAPK2 (GST)
MAPKAPK2 (His)   MAPKAPK3   MAPKAPK5
MARK1   MARK2   MARK3
MARK4   MEK1   MEK1 (EE)
MEK2 (GST)   MEK2 (His)   MEKK1
MEKK2   MEKK3   MEKK6
MELK   MET (h)   MET (M1250T)
MET (r)   MINK1   MLCK
MLK1   MLK2   MLK3
MNK1   MNK2   MRCK alpha
MRCK beta   MSK1   MSK2
MSSK1   MST1   MST3
MST4   MUSK   MYLK2
MYLK3   MYO3 beta   MYT1
NDR   NDR2(STK38L)   NEK11
NEK2   NEK3   NEK4
NEK6   NEK7   NEK9
NIK   NLK   NUAK1
NUAK2   p38 alpha   p38 beta
p38 delta   p38 gamma   p70S6K
p70S6Kb   PAK1   PAK1/CDC42
PAK2   PAK3   PAK4
PAK6   PAK7   PASK
PDE10A   PDE11A   PDE1A
PDE1B   PDE1C   PDE2A
PDE3A   PDE3B   PDE4A
PDE4B   PDE4C   PDE4D
PDE5A   PDE6A   PDE6B
PDE6C   PDE7A   PDE7B
PDE8A   PDE8B   PDE9A
PDGFR alpha (D842V)   PDGFR alpha (h)   PDGFR alpha (m)
PDGFR alpha (T674I)   PDGFR beta   PDHK1
PDHK2   PDHK3   PDHK4
PDK1   PHKG1   PHKG2
PI3K (p110 alpha(E545K)/p85 alpha)   PI3K (p110 alpha/p55 gamma)     PI3K (p110 alpha/p65 alpha)
PI3K (p110 alpha/p85 alpha) (h)   PI3K (p110 alpha/p85 alpha) (m)   PI3K (p110 beta/p85 alpha)
PI3K (p110 beta/p85 beta)   PI3K (p110 delta/p85 alpha)   PI3K (p120 gamma)
PI3K (Vps34/Vps15)   PI4K2A   PI4K2B
PI4KA   PI4KB   PIK3C2G  
PIK3C3 (Vps34)     PIM1   PIM2
PIM3   PIP4K2A   PIP4K2B  
PIP4K2C   PIP5K1A   PIP5K1B
PIP5K1C   PKAc alpha   PKAc beta
PKAc gamma   PKC alpha (h)   PKC alpha (x)
PKC beta I   PKC beta II   PKC delta
PKC epsilon   PKC eta   PKC gamma
PKC iota   PKC mu   PKC nu
PKC theta   PKC zeta   PKD2
PKN1/PRK1   PKN2/PRK2   PKN3/PKR3
PLK1   PLK2   PLK3
PLK4   PLK4     PRKG1
PRKG2   PRKX   PTPN1 (PTP1B)
PTPN11 (SHP2)   PTPN12 (PTP-PEST)   PTPN13 (FAP-1)
PTPN2 (TC-PTP)   PTPN6 (SHP1)   PTPN7 (LC-PTP)
PTPRA (LRP)   PTPRC (CD45) (h)   PTPRC (CD45) (m)
PTPRF (LAR)   PTPRS (PTP- sigma)   PYK2
QIK   RAF1   RAF1(EE)
RET   RET (V804L)     RIPK2
RIPK3     RIPK5   ROCK1
ROCK2 (GST)   ROCK2 (His)   RON
ROR2   ROS1   RSK1
RSK2   RSK3   RSK4
SGK1   SGK2   SGK3
SIK   SIRT1   SIRT2
SIRT3   SIRT5   SIRT6
SIRT7   SLK   SOK1
SPHK1   SPHK2   SRC (h)
SRC (v)   SRMS   SRPK1
SRPK2   STK3   STK32B (YANK2)
STK32C(YANK3)   STK33   STK39 (STLK3)
SYK   TAK1-TAB1   TAOK1
TAOK2   TAOK3   TBK1
TEC   TESK1   TGF betaR1 (ALK5)
TGF betaR2   TIE 2   TLK1
TLK2   TNIK   TOPK
TRKA   TRKB   TRKC
TSSK1B   TSSK2   TTBK2
TTK   TXK   TYK2 (JTK1)
TYRO3   ULK1   ULK2
ULK3   VRK1   VRK2
WEE1   WNK1   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

 


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  TNF-alpha   RANTES (CCL5)  
  PDGF   PAK2 Protein  
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  p38 beta, Active   p38 alpha, Active  
  VEGF-C   OPG  
  LMTK3 Protein   LATS1, Active  
  IL-18   IFN-gamma  
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  ALK7 Protein   CDK7, Unactive  
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