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Isoforms Recommended:	Chk1

Results for "

Chk1

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Adrenergic Receptor (1) Akt (2) AMPK (1) Amyloid-β (1) Anaplastic lymphoma kinase (ALK) (1) Apoptosis (16) ATM/ATR (2) Aurora Kinase (1) Autophagy (2) Biochemical Assay Reagents (1) c-Fms (1) c-Kit (1) c-Myc (1) Calmodulin (2) Casein Kinase (2) CDK (5) Checkpoint Kinase (Chk) (62) Choline Kinase (1) DNA/RNA Synthesis (2) Drug Intermediate (1) Drug Isomer (1) Early 2 Factor (E2F) (1) EGFR (1) Endogenous Metabolite (1) ERK (1) FGFR (1) FLT3 (5) MAP3K (2) MAPKAPK2 (MK2) (3) MDM-2/p53 (2) Microtubule/Tubulin (1) PDGFR (1) Phosphatase (1) PI3K (1) Pim (1) PKC (2) PROTACs (2) RET (1) Small Interfering RNA (siRNA) (2) Src (1) STAT (1) Trk Receptor (1) VEGFR (1) Wee1 (4)
By Research Areas:	Cancer (66) Cardiovascular Disease (2) Inflammation/Immunology (3) Neurological Disease (1)
Oligonucleotides:	Mouse Pre-designed siRNA Sets (1) Human Pre-designed siRNA Sets (1) siRNAs (2)

Inhibitors & Agonists

Biochemical Assay Reagents

Peptides

Recombinant Proteins

Antibodies

Oligonucleotides

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-131446

Chk1-IN-5 1 Publications Verification	Checkpoint Kinase (Chk)	Cancer
Chk1-IN-5 is a potent checkpoint kinase 1 (Chk1) inhibitor. Chk1-IN-5 inhibits Chk1 phosphorylation and inhibits tumor growth in colon cancer xenograft model ^[1].

HY-128601

CHK1-IN-3	Checkpoint Kinase (Chk)	Cardiovascular Disease Cancer
CHK1-IN-3 is a potent and selective *CHK1* inhibitor with an IC₅₀ of 0.4 nM. CHK1-IN-3 effectively inhibits the growth of malignant hematopathy cell lines and displays low affinity for hERG (IC₅₀ > 40 μM). CHK1-IN-3 significantly suppresses the tumor growth in vivo. CHK1-IN-3 can be used for the study of hematologic malignancies ^[1].

HY-128766A

CHK1-IN-4 hydrochloride	Checkpoint Kinase (Chk)	Cancer
CHK1-IN-4 hydrochloride (Compound 3) is a potent checkpoint kinase 1 (chk1) inhibitor, and potently inhibits chk1 phosphorylation in the tumor cells. CHK1-IN-4 hydrochloride has anti-tumor activity ^[1].

HY-139901

Chk1-IN-6	Checkpoint Kinase (Chk)	Cancer
Chk1-IN-6 is a selective and orally active *Chk1* inhibitor with an IC₅₀ of 16.1 nM. Chk1-IN-6 shows antiproliferative activity of MV-4-11 cells. Chk1-IN-6 exerts effective response in the MV-4-11 xenograft mouse model. Chk1-IN-6 exhibits synergistic anticancer effect with Gemcitabine (HY-17026). Chk1-IN-6 can be used in the research of cancers such as acute myeloid leukemia and colorectal adenocarcinoma ^[1].

HY-103367

CHK1-IN-7	Checkpoint Kinase (Chk)	Cancer
CHK1-IN-7 (Compound 10c) is a potent human *CHK1* inhibitor. CHK1-IN-7 shows no single agent effect, potentiates the antiproliferative effect of Gemcitabine HY-17026 in both prostate and breast cancer cell lines. CHK1-IN-7 can be used for the research of cancer ^[1].

HY-171759

CHK1-IN-11	Checkpoint Kinase (Chk)	Cancer
CHK1-IN-11 (Compound 1) is an orally active, checkpoint kinase 1 (CHK1) inhibitor. CHK1-IN-11 is useful for the study of cancers with oncogene amplification ^[1].

HY-171785

CHK1-IN-12	Checkpoint Kinase (Chk) Apoptosis	Cancer
CHK1-IN-12 (Compound example 1-5) is an orally active and highly selective checkpoint kinase 1 (CHK1) inhibitor with in vitro enzyme IC₅₀≤10 nM and cellular IC₅₀≤50 nM. CHK1-IN-12 inhibits the phosphorylation activity of CHK1 kinase to block the DNA damage response pathway, inducing tumor cell cycle arrest and apoptosis. CHK1-IN-12 is promising for research of cancers ^[1].

HY-177027

CHK1-IN-13	Checkpoint Kinase (Chk)	Cancer
CHK1-IN-13 (Compound 38) is a checkpoint kinase 1 (Chk1) inhibitor with an IC₅₀ of 10-50  nM. CHK1-IN-13 has anticancer activity, and can be used for the research of cancers, such as breast, ovarian and prostate cancer ^[1].

HY-155798

CHK1-IN-8	Checkpoint Kinase (Chk)	Cancer
CHK1-IN-8 (example 3-2) is a *Chk1* inhibitor with an IC₅₀ of <10 nM for human Chk1. CHK1-IN-8 can be used for the study of cancer ^[1].

HY-128766

CHK1-IN-4	Checkpoint Kinase (Chk)	Cancer
CHK1-IN-4 (Compound 3) is a potent checkpoint kinase 1 (chk1) inhibitor, and potently inhibits chk1 phosphorylation in the tumor cells. CHK1-IN-4 has anti-tumor activity ^[1].

HY-161383

CHK1-IN-9	Checkpoint Kinase (Chk)	Cancer
CHK1-IN-9 (compound 11) is an orally active *CHK1* inhibitor with an IC₅₀ value of 0.55 nM. CHK1-IN-9 can enhance the effect of DNA-damaging drugs on tumor cells. CHK1-IN-9 has synergistic anticancer effects with Gemcitabine (HY-17026) ^[1].

HY-111369

CHK1-IN-2	Checkpoint Kinase (Chk)	Cancer
CHK1-IN-2 is a checkpoint kinase 1 *(CHK1)* inhibitor, with an IC₅₀ of 6 nM.

HY-161108

*PROTAC Chk1* degrader-1**	PROTACs Checkpoint Kinase (Chk)	Cancer
PROTAC Chk1 degrader-1 (Compound PROTAC-2 ) is a potent PROTAC-targeted degrader of *Chk1* with a DC₅₀ of 1.33 μM. PROTAC Chk1 degrader-1 can be used in cancer research ^[1].

HY-162367

*FLT3/CHK1-IN-2*	FLT3 Checkpoint Kinase (Chk)	Cancer
FLT3/CHK1-IN-2 (Compound 30) is a dual inhibitor of FLT3 and *CHK1, with IC₅₀s of 25.63, 16.39, 22.80 nM for CHK1, FLT3-WT, and FLT-D835Y respectively. FLT3/CHK1-IN-2* has favorable oral PK properties and kinase selectivity. FLT3/CHK1-IN-2 can be used for research of acute myeloid leukemia (AML) ^[1].

HY-178858

*PROTAC FLT3/CHK1* Degrader-1**	PROTACs FLT3 Checkpoint Kinase (Chk) STAT ERK c-Myc Akt	Cancer
PROTAC FLT3/CHK1 Degrader-1 is a PROTAC *FLT3/CHK1* degrader, with DC₅₀ values of 5.88 nM (FLT3) and 4.17 nM (CHK1), respectively. PROTAC FLT3/CHK1 Degrader-1 can inhibit the phosphorylation of FLT3 downstream signaling effectors STAT5 (Tyr694), AKT (Ser473), and ERK (Tyr204), downregulate the protein level of c-Myc and maintain the expression of p53 protein. PROTAC FLT3/CHK1 Degrader-1 induces apoptosis in MV-4-11 cells. PROTAC FLT3/CHK1 Degrader-1 shows significant anti-tumor efficacy in mice bearing MV-4-11 subcutaneous xenografts. PROTAC FLT3/CHK1 Degrader-1 can be used for the study of acute myeloid leukemia (AML). (Pink: FLT3/CHK1 ligand (HY-178869 ), Blue: CRBN Ligand (HY-W093272), Black: Linker, E3 ligase ligand-linker conjugate (HY-W998238)) ^[1].

HY-159707

MCL1020	Checkpoint Kinase (Chk)	Cardiovascular Disease Cancer
MCL1020 is a *CHK1* inhibitor with an IC₅₀ of 1.61 μM. MCL1020 properly occupies the ATP pocket by interacting with a diverse range of the sites of CHK1 kinase. MCL1020 can be used for the study of hematologic malignancies ^[1].

HY-161622

K1586	Checkpoint Kinase (Chk)	Cancer
K1586 is an amidine derivative that efficiently targets *Chk1. K1586 enhances the degradation of Chk1* that sensitizes colorectal cancer cells to ionizing radiation. K1586 shows anticancer effects ^[1].

HY-P10574

Phosphorylated CHKtide	Checkpoint Kinase (Chk)	Cancer
Phosphorylated CHKtide is a synthetic peptide substrate derived from CDC25C, which is phosphorylated by *CHK1/CHK2* in one of the DNA repair pathways. Phosphorylated CHKtide is used in the assays of cell cycle checkpoint kinases 1 and 2 (CHK1/CHK2) and salt-inducible kinases (SIKs) ^[1].

HY-112927

MU380	Checkpoint Kinase (Chk)	Cancer
MU380 is a potent and selective *CHK1* inhibitor that induces apoptosis and has anticancer activity ^[1].

HY-P5961

Chktide	Checkpoint Kinase (Chk)	Cancer
Chktide is a substrate for CHK1 and CHK2. Chktide can be used in kinase assays ^[1] .

HY-10032

PF 477736 5 Publications Verification PF 00477736	Checkpoint Kinase (Chk) VEGFR Src c-Fms Aurora Kinase FGFR FLT3 RET CDK	Cancer
PF 477736 (PF 00477736) is a potent, selective and ATP-competitive inhibitor of *Chk1, with a K_i* of 0.49 nM, it is also a *Chk2* inhibitor, with a K_i of 47 nM. PF 477736 shows <100-fold selectivity for Chk1 over VEGFR2, Fms, Yes, Aurora-A, FGFR3, Flt3, and Ret (IC₅₀=8 (K_i), 10, 14, 23, 23, 25, and 39 nM, respectively). PF 477736 can enhance Gemcitabine antitumor activity in vitro and in vivo ^[1] .

HY-107407

SB-218078 5 Publications Verification	Checkpoint Kinase (Chk) CDK PKC Apoptosis	Cancer
SB-218078 is a potent, selective, ATP-competitive and cell-permeable checkpoint kinase 1 (Chk1) inhibitor that inhibits *Chk1* phosphorylation of cdc25C with an IC₅₀ of 15 nM. SB-218078 is less potently inhibits Cdc2 (IC₅₀ of 250 nM) and PKC (IC₅₀ of 1000 nM). SB-218078 causes apoptosis by DNA damage and cell cycle arrest ^[1] .

HY-112167B

GDC0575 hydrochloride ARRY-575 hydrochloride; RG7741 hydrochloride	Checkpoint Kinase (Chk)	Inflammation/Immunology Cancer
GDC0575 (ARRY-575) hydrochloride is a highly-selective and orally active *Chk1* (IC₅₀=1.2 nM) inhibitor. GDC0575 (ARRY-575) hydrochloride can be used for colitis-associated cancer (CAC) and colitis research ^[1].

HY-155195

*FLT3/CHK1-IN-1*	FLT3	Cancer
FLT3/CHK-IN-1 (Compound 18) is a dual inhibitor of FLT3/CHK1. FLT3/CHK-IN-1 is more than 1700 times more selective to c-KI T and greatly reduces hERG affinity with an IC₅₀ value of 58.4 μM. FLT3/CHK-IN-1 inhibits tumor growth in mouse xenotransplantation models inoculated with MV-4-11 cells ^[1].

HY-119699

PV1115	Checkpoint Kinase (Chk)	Cancer
PV1115 is a potent and highly selective *Chk2* inhibitor with an IC₅₀ of 0.14 nM, 66000 nM, >100000 nM for Chk2, Chk1 and RSK2, respectively. PV1115 is situated within the ATP-binding pocket of Chk2 ^[1].

HY-19926

GDC-0425 RG-7602	Checkpoint Kinase (Chk)	Cancer
GDC-0425 (RG-7602) is an orally available, highly selective small molecule *ChK1* inhibitor. GDC-0425 can be used for the research of various malignancies ^[1] .

HY-14720

Rabusertib 10+ Cited Publications LY2603618; IC-83	Checkpoint Kinase (Chk) Autophagy	Cancer
Rabusertib (LY2603618) is a potent and selective inhibitor of *Chk1* with an IC₅₀ of 7 nM.

HY-136270

Gartisertib 4 Publications Verification VX-803; M4344; ATR inhibitor 2	ATM/ATR	Cancer
Gartisertib (VX-803) is an ATP-competitive, orally active, and selective ATR inhibitor, with a K_i of <150 pM. Gartisertib potently inhibits ATR-driven phosphorylated checkpoint kinase-1 (Chk1) phosphorylation with an IC₅₀ of 8 nM. Antitumor activity ^[1] .

HY-U00345

CHK-IN-1	Checkpoint Kinase (Chk)	Cancer
CHK-IN-1 is an inhibitor of *CHK1* and *CHK2*, with anti-proliferative activities.

HY-18958

CCT245737 3 Publications Verification SRA737	Checkpoint Kinase (Chk)	Cancer
CCT245737 (SRA737) is an orally active and seletive *Chk1* inhibitor, with an IC₅₀ of 1.3 nM.

HY-10992

AZD-7762 20+ Cited Publications	Checkpoint Kinase (Chk)	Cancer
AZD-7762 is a potent ATP-competitive checkpoint kinase (Chk) inhibitor in with an IC₅₀ of 5 nM for Chk1.

HY-10992A

AZD-7762 hydrochloride 20+ Cited Publications	Checkpoint Kinase (Chk)	Cancer
AZD-7762 hydrochloride is a potent ATP-competitive checkpoint kinase (Chk) inhibitor in with an IC₅₀ of 5 nM for *Chk1*.

HY-124731

PD-321852	Checkpoint Kinase (Chk)	Cancer
PD-321852 is a *Chk1* inhibitor, with IC₅₀ of 5 nM. PD-321852 can be used in anti-cancer research ^[1].

HY-112167A

GDC-0575 dihydrochloride 5+ Cited Publications ARRY-575 dihydrochloride; RG7741 dihydrochloride	Checkpoint Kinase (Chk)	Cancer
GDC-0575 dihydrochloride (ARRY-575 dihydrochloride) is an orally bioavailable *CHK1* inhibitor, with an IC₅₀ of 1.2 nM, and has antitumor activity.

HY-18958A

(S)-CCT245737 (S)-SRA737	Checkpoint Kinase (Chk)	Others
(S)-CCT245737 ((S)-SRA737) is a potent and selective oral inhibitor of checkpoint kinase 1 (CHK1).

HY-P10367

Ziptide	MAPKAPK2 (MK2) Checkpoint Kinase (Chk) AMPK	Others
Ziptide is a substrate for MAPK activated protein kinase 2 (MAPKAPK2, K_m = 5 μM), MAPKAPK3 (K_m = 30 μM), PARK (K_m = 40 μM), checkpoint kinase 1 (Chk1, K_m = 5 μM), AMP-activated protein kinase (AMPK, K_m = 75 μM), and calcium/calmodulin-dependent protein kinase II (CamKII, K_m = 300 μM) ^[1].

HY-112167

GDC-0575 5+ Cited Publications ARRY-575; RG7741	Checkpoint Kinase (Chk)	Cancer
GDC-0575 (ARRY-575, RG7741) is a highly-selective oral small-molecule *Chk1* inhibitor with an IC₅₀ of 1.2 nM.

HY-18942

VER-00158411	Checkpoint Kinase (Chk)	Cancer
VER-00158411 is a checkpoint kinase 1 (CHK1) and *CHK2* inhibitor with IC₅₀ values of 4.4 nM and 4.5 nM, respectively ^[1].

HY-148962

LY2880070	Checkpoint Kinase (Chk)	Cancer
LY2880070 is an orally active *CHK1* inhibitor, IC₅₀ ＜ 1 nM. LY2880070 can be used as an anticancer agent for combination with DNA damaging agents ^[1] .

HY-18175

CCT244747 4 Publications Verification	Checkpoint Kinase (Chk)	Cancer
CCT244747 is a potent, orally bioavailable and highly selective *CHK1* inhibitor, with an IC₅₀ of 7.7 nM; CCT244747 also abrogates G2 checkpoint with an IC₅₀ of 29 nM.

HY-15532B

SCH900776 (S-isomer) MK-8776 S-isomer	Drug Isomer	Cancer
SCH900776 S-isomer is the S-isomer of SCH900776. SCH900776 is a potent, selective and orally bioavailable inhibitor of checkpoint kinase1 (Chk1) with IC₅₀ of 3 nM.

HY-100195

SAR-020106 1 Publications Verification	Checkpoint Kinase (Chk)	Cancer
SAR-020106 is an ATP-competitive, potent, and selective *CHK1* inhibitor with an IC₅₀ of 13.3 nM for human CHK1. SAR-020106 shows excellent selectivity over CHK2. SAR-020106 significantly enhances the cell killing of Gemcitabine and SN38 by 3- to 29-fold in several colon tumor lines and in a p53-dependent fashion. SAR-020106 can enhance antitumor activity with selected anticancer agents ^[1] .

HY-13263

CHIR-124 3 Publications Verification	Checkpoint Kinase (Chk) FLT3 PDGFR Apoptosis	Cancer
CHIR-124 is a potent and selective *Chk1* inhibitor with IC₅₀ of 0.3 nM, and also potently targets PDGFR and FLT3 with IC₅₀s of 6.6 nM and 5.8 nM.

HY-40029

(S)-1-Boc-3-aminopiperidine (S)-(+)-3-Amino-1-boc-piperidine	Biochemical Assay Reagents Drug Intermediate Checkpoint Kinase (Chk) PI3K	Others
(S)-1-Boc-3-aminopiperidine is a key intermediate for the synthesis of various novel inhibitors, such as *CHK1* inhibitors and PI3Kδ inhibitors ^[1].

HY-106009

VRX0466617	Checkpoint Kinase (Chk)	Cancer
VRX0466617 is a selective and ATP-competitive *Chk2* inhibitor with an IC₅₀ of 120 nM and a K_i of 11 nM. VRX0466617 does not inhibit the related Chk1 activity. VRX0466617 can be used in the study of cancer.

HY-13925

PD0166285 5+ Cited Publications	Wee1 Apoptosis	Cancer
PD0166285, a substrate of P-gp, is a *WEE1* inhibitor and a weak *Myt1* inhibitor with IC₅₀ values of 24 and 72 nM, respectively. PD0166285 exhibits an IC₅₀ of 3.433 μM for Chk1 ^[1].

HY-13925A

PD0166285 dihydrochloride	Wee1 Apoptosis	Cancer
PD0166285 dihydrochloride, a substrate of P-gp, is a *WEE1* inhibitor and a weak *Myt1* inhibitor with IC₅₀ values of 24 and 72 nM, respectively. PD0166285 dihydrochloride exhibits an IC₅₀ of 3.433 μM for Chk1 ^[1].

HY-18961

PD 407824	Checkpoint Kinase (Chk) Wee1	Inflammation/Immunology Cancer
PD 407824 is a checkpoint kinase *Chk1* and *WEE1* inhibitor with IC₅₀s of 47 and 97 nM, respectively. PD 407824 is a chemical BMP sensitizer and increases the sensitivity of cells to sub-threshold amounts of BMP4 ^[1] .

HY-15532

SCH900776 10+ Cited Publications MK-8776	Checkpoint Kinase (Chk)	Cancer
SCH900776 (MK-8776) is a potent, selective and orally bioavailable inhibitor of checkpoint kinase1 (Chk1) with an IC₅₀ of 3 nM. SCH900776 shows 50- and 500-fold selectivity over CDK2 and Chk2, respectively ^[1] .

HY-122198

ML367	Checkpoint Kinase (Chk)	Cancer
ML367 is a potent inhibitor of ATPase family AAA domain-containing protein 5 (ATAD5) stabilization, acts as a probe molecule that has low micromolar inhibitory activity. ML367 blocks DNA repair pathways, suppresses general DNA damage responses including RPA32-phosphorylation and CHK1-phosphorylation in response to UV irradiation ^[1].

Cat. No.	Product Name	Target	Research Area

HY-16129A

CBP-501 acetate	Calmodulin MAP3K MAPKAPK2 (MK2) Checkpoint Kinase (Chk)	Cancer
CBP-501 acetate, a cell-permeable calmodulin-binding peptide and a G2-abrogating drug candidate, inhibits the activity of multiple Ser ²¹⁶-specific kinases, such as MAPKAP-K2, *C-Tak1, CHK1* and *CHK2*, with IC₅₀ values of 0.9 μM, 1.4 μM 3.4 μM and 6.5 μM, respectively. CBP-501 acetate is used for various types of cancer ^[1] .

HY-P10574

Phosphorylated CHKtide	Checkpoint Kinase (Chk)	Cancer
Phosphorylated CHKtide is a synthetic peptide substrate derived from CDC25C, which is phosphorylated by *CHK1/CHK2* in one of the DNA repair pathways. Phosphorylated CHKtide is used in the assays of cell cycle checkpoint kinases 1 and 2 (CHK1/CHK2) and salt-inducible kinases (SIKs) ^[1].

HY-P5961

Chktide	Checkpoint Kinase (Chk)	Cancer
Chktide is a substrate for CHK1 and CHK2. Chktide can be used in kinase assays ^[1] .

HY-P10367

Ziptide	MAPKAPK2 (MK2) Checkpoint Kinase (Chk) AMPK	Others
Ziptide is a substrate for MAPK activated protein kinase 2 (MAPKAPK2, K_m = 5 μM), MAPKAPK3 (K_m = 30 μM), PARK (K_m = 40 μM), checkpoint kinase 1 (Chk1, K_m = 5 μM), AMP-activated protein kinase (AMPK, K_m = 75 μM), and calcium/calmodulin-dependent protein kinase II (CamKII, K_m = 300 μM) ^[1].

HY-16129

CBP-501	Calmodulin Checkpoint Kinase (Chk) MAPKAPK2 (MK2) MAP3K	Cancer
CBP-501, a cell-permeable calmodulin-binding peptide and a G2-abrogating drug candidate, inhibits the activity of multiple Ser ²¹⁶-specific kinases, such as MAPKAP-K2, *C-Tak1, CHK1* and *CHK2*, with IC₅₀ values of 0.9 μM, 1.4 μM 3.4 μM and 6.5 μM, respectively. CBP-501 is used for various types of cancer ^[1] .

Recombinant Proteins Recommended:

Checkpoint Kinase 1 (Chk1)

Species:	Human (1) Mouse (1)
Tag:	His (1) GST (2)
Source:	Sf9 insect cells (2)

Cat. No.	Compare	Product Name	Species	Source

HY-P75672

	Chk1 Protein, Human (sf9, GST) Serine/threonine-protein kinase Chk1; Chek1; Chk1	Human	Sf9 insect cells
	The serine/threonine protein kinase CHK1 is essential for checkpoint-mediated cell cycle arrest and DNA repair. It may negatively regulate cell cycle progression and maintain genomic integrity during the normal cell cycle. The kinase recognizes the consensus sequence [R-X-X-S/T] and phosphorylates CDC25A, CDC25B, and CDC25C. Phosphorylation of CDC25A inhibits its activity and promotes proteolysis, while increasing tyrosine phosphorylation of CDK-cyclin complexes. In addition, the kinase phosphorylates RAD51 and TP53, enhancing DNA repair and cell cycle arrest. Chk1 Protein, Human (sf9, GST) is the recombinant human-derived Chk1 protein, expressed by Sf9 insect cells , with N-GST labeled tag.

HY-P74253

	Chk1 Protein, Mouse (sf9, His-GST) Serine/threonine-protein kinase Chk1; Chek1; Chk1	Mouse	Sf9 insect cells
	Chk1 is a serine/threonine protein kinase that critically coordinates checkpoint-mediated cell cycle arrest and DNA repair in response to DNA damage or unreplicated DNA. It negatively regulates unperturbed cell cycle progression and protects genome integrity by phosphorylating key targets such as CDC25A, CDC25B, CDC25C, RAD51, TP53, histone H3.1, RB1, SPRTN, TLK1 and FANCE. Chk1 Protein, Mouse (sf9, His-GST) is the recombinant mouse-derived Chk1 protein, expressed by Sf9 insect cells , with N-His, N-GST labeled tag.

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HY-P80617

	Chk1 Antibody CHEK1; Chk1; Serine/threonine-protein kinase Chk1; Chk1 checkpoint homolog; Cell cycle checkpoint kinase; Checkpoint kinase-1	WB, ICC/IF, IP	Human, Mouse, Rat
	Chk1 Antibody is a Rabbit-derived and non-conjugated IgG polyclonal antibody, targeting to Chk1.

HY-P80082

	Chk1 Antibody (YA505) 1 Publications Verification	WB, ICC/IF, IHC-P, FC	Human, Mouse
	Chk1 Antibody (YA505) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to Chk1.

HY-P80455

	*Phospho-Chk1* (Ser296) Antibody (YA216)** 1 Publications Verification	WB, IHC-P	Human
	Phospho-Chk1 (Ser296) Antibody (YA216) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to Phospho-Chk1 (Ser296).

HY-P86303

	Chk1 Antibody (YA5995) CHEK1; Chk1; Serine/threonine-protein kinase Chk1; Chk1 checkpoint homolog; Cell cycle checkpoint kinase; Checkpoint kinase-1	WB, ICC/IF, IP, ELISA	Human, Mouse, Rat
	Chk1 Antibody (YA5995) is a Rabbit-derived and non-conjugated IgG monoclonal antibody, targeting to Chk1.

HY-P83808

	Chk1 Antibody (YA3505) CHEK1	WB, ELISA	Human, Mouse
	Chk1 Antibody (YA3505) is a Mouse-derived and non-conjugated IgG1 monoclonal antibody, targeting to Chk1.

HY-P87896

	*Phospho-Chk1* (Ser317) Antibody (YA7581)**	WB, IHC, ICC/IF, IP, ELISA	Human, Mouse, Rat

HY-P87936

	*Phospho-Chk1* (Ser345) Antibody (YA7621)**	WB, ICC/IF, ELISA	Human, Mouse, Rat

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