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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   BUB1  
BUB1B     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
CASK     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
EGFR (L861Q)     EGFR (T790M)     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)
FASTK     FER   FES
FGFR1 (FLT2)   FGFR1 (V561M)   FGFR2
FGFR3   FGFR3 (K650E)   FGFR4
FGR   FLT (D835Y)   FLT1
FLT3   FLT4   FMS
FRK   FYN A   GCK
GRK1   GRK2   GRK3  
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
KSR1     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)   NEK1     NEK11
NEK2   NEK3   NEK4
NEK5     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
PIK3C2A     PIK3C2G   PIK3C3 (Vps34)
PIM1   PIM2   PIM3
PIP4K2A   PIP4K2B   PIP4K2C
PIP5K1A   PIP5K1B   PIP5K1C
PIP5K3     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   PP1A  
PP1B     PP2Aalpha     PP2Calpha  
PP2Cgamma     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)   PTPRE (PTP-epsilon)
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   TNK1  
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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