Search Result

Search Results for " pc3 "

Targets

Compounds

Natural Products

Recombinant Proteins

Cat No.	Product Name	Synonyms	Targets
T12928	SK33		Androgen Receptor
	SK33 is a potent and tissue selective anti-androgen agent. SK33 reduces androgen receptor (AR) transcriptional activity.		Androgen Receptor
T1267	Abacavir	Epzicom,Ziagen,Abacavir sulfate	Apoptosis , HIV Protease , Reverse Transcriptase
	Abacavir (Ziagen) is a nucleoside reverse transcriptase inhibitor analog of guanosine. This agent decreases HIV viral loads, retards or prevents the damage to the immune system, and reduces the risk of developing AIDS.		Apoptosis , HIV Protease , Reverse Transcriptase
T1448	Dasatinib	BMS-354825	Apoptosis , Bcr-Abl , Src , c-Kit , Autophagy
	Dasatinib (BMS-354825) is a tyrosine kinase inhibitor that inhibits Src and Bcr-Abl (Ki=16/30 pM) and is orally active and ATP-competitive. Dasatinib has antitumor activity and is used in the treatment of leukemia and ly...		Apoptosis , Bcr-Abl , Src , c-Kit , Autophagy
T6967	RHPS4	RHPS 4 methosulfate,NSC714187	Apoptosis , Telomerase
	RHPS4 (RHPS 4 methosulfate) is a potent inhibitor of Telomerase at submicromolar.		Apoptosis , Telomerase
T6367	Abacavir sulfate	Abacavir Hemisulfate,1592U89,ABC sulfate,Ziagen	Apoptosis , HIV Protease , Reverse Transcriptase
	Abacavir sulfate (Ziagen) , a nucleoside analogue, effectively utilize its antiviral activity		Apoptosis , HIV Protease , Reverse Transcriptase
T1448L	Dasatinib monohydrate	BMS-354825 Monohydrate	Apoptosis , Bcr-Abl , Src , c-Kit , Ephrin Receptor , Autophagy
	Dasatinib monohydrate (BMS-354825 Monohydrate) is an orally bioavailable synthetic small molecule-inhibitor of SRC-family protein-tyrosine kinases. Dasatinib monohydrate binds to and inhibits the growth-promoting activit...
T79054	TRPC3/6-IN-2
	TRPC3/6-IN-2 is a potent inhibitor of TRPC3 and TRPC6, exhibiting IC50 values of 16 nM for TRPC3 and 29.8 nM for TRPC6, respectively [1].
T29113	VPC32183	VPC-32183,VPC 32183
	VPC32183 is a competitive antagonist of LPA1 and LPA3 receptors.
T61407	TRPC3/6-IN-1
	TRPC3/6-IN-1 is a highly potent and selective inhibitor that specifically blocks the activity of the canonical transient receptor channels TRPC3 and TRPC6. It exhibits a significant blocking potency against the human iso...
T35071	VPC32179	VPC 32179,VPC-32179
	VPC32179 is a bioactive chemical.
T10657	C75	C-75	Fatty Acid Synthase
	C75 is an inhibitor synthetic fatty-acid synthase (FASN) and inhibits prostate cancer cells PC3 (IC50: 35 μM).		Fatty Acid Synthase
T35666	PRGL493		Others
	PRGL493 is an inhibitor of long-chain acyl-CoA synthetase 4 (ACSL4).1It inhibits formation of arachidonoyl-CoA (AA-CoA) from arachidonic acid in, as well as the proliferation and migration of, PC3 and MDA-MB-231 cancer c...		Others
TP1895L1	KYL acetate(676657-00-4 free base)		Ephrin Receptor
	KYL acetate is an EphA4 receptor tyrosine kinase inhibitor (Kd = 0.8 μM); inhibits EphA4-EphrinA5 interactions (IC50 = 6.34 μM). Prevents AβO induced synaptic damage, dendritic spine loss and prevents the blocking of LTP...		Ephrin Receptor
T29110	VPC-13163	2,3-dihydro-2,3'-Bi-1H-indole,VPC13163,NSC52361,NSC 52361,VPC 13163	Others
	VPC-13163 (NSC-52361) has strong anti-proliferative activity against LNCaP and Enzalutamide-resistant prostate cancer cell lines (MR49F) whereas it did not affect the growth of AR independent PC3 cell line. It also inhib...		Others
T3989	SMI-16a	PIM1/2 Kinase Inhibitor VI	Pim
	SMI-16a (PIM1/2 Kinase Inhibitor VI) , a cell-permeable thiazolidinedione compound, acts as an effective, ATP-competitive inhibitor against Pim-1/2 kinases (IC50: 150/20 nM) while exhibiting little or no activity against...		Pim
T10656	Trans-C75	(±)-C75	Others , Fatty Acid Synthase
	trans-C75 ((±)-C75) is an enantiomer of C75. C75 is an inhibitor of fatty-acid synthase (FASN).		Others , Fatty Acid Synthase
T36991	Monascuspiloin
	Monascuspiloin is a fungal metabolite that has been found inM. pilosusM93-fermented rice.1It induces endoplasmic reticulum stress and autophagy in PC3 prostate cancer cells. Monascuspiloin (15-45 μM) decreases viability ...
T64222	Antitumor agent-55
	Antitumor agent-55 (compound 5q) is a potent antitumour agent that effectively inhibits PC3 (IC50: 0.91 μM). antitumor agent-55 blocks the G1/S phase of the PC3 cell cycle, induces apoptosis, inhibits cell migration and ...
T72468	Anticancer agent 25
	Anticancer agent 25 demonstrates the highest level of cytotoxic effectiveness on PC3 cells, achieving an IC 50 value of 0.19 μM.
T68441	SABRAC
	SABRAC inhibits acid ceramidase in PC3 MC metastatic prostate cancer cells (IC50 = <1 µM), as well as induces accumulation of ceramides in the same cells.
T78051	Necrocide 1		Others
	Necrocide 1 (compound (S)-38), a potent anticancer agent, exhibits antiproliferative activity with IC50 values of 0.48 nM for MCF-7 and 2 nM for PC3 cancer cell lines, respectively [1].		Others
T35855	AAA
	AAA is an antagonist of G protein-coupled receptor 75 (GPR75).1It increases basal GPR75 protein levels and inhibits 20-HETE-induced reductions in GPR75 protein levels in PC3 cells. AAA (5 and 10 μM) also reduces 20-HETE-...
T36628	PROTAC BRD4 Degrader-8	PROTAC BRD4 Degrader-8
	PROTAC BRD4 Degrader-8 is a potent BRD4 inhibitor, with IC50s of 1.1 nM and 1.4 nM for BRD4 BD1 and BD2, respectively. PROTAC BRD4 Degrader-8 is capable of potently degrading the BRD4 protein in PC3 prostate cancer cells...
T10924	Cysteine protease inhibitor-2		Cysteine Protease
	Cysteine protease inhibitor 2 is a cysteine protease inhibitor. Cysteine protease inhibitor 2 inhibited DCT116 and PC3 cells with GI50 values of 6.5 μM and 4.4 μM, respectively.		Cysteine Protease
T74299	MS5033
	MS5033 is a potent proteolysis-targeting chimera (PROTAC) that effectively degrades AKT (also known as protein kinase B), exhibiting a half-maximal degradation concentration (DC50) of 430 nM in PC3 cells [1].
T70962	MHY219
	MHY219 is a novel HDAC inhibitor. MHY219 induces apoptosis via up-regulation of androgen receptor expression in human prostate cancer cells. MHY219 was shown to enhance the cytotoxicity on DU145 cells (IC50, 0.36 μM) whe...
T83007	Antitumor agent-120
	Antitumor agent-120 (compound 1), a flavonoid derived from Kudzu root, exhibits negligible inhibitory effects on LNCaP and PC3 cancer cells, with IC50 values exceeding 50 μM [1].
T61902	Anticancer agent 69
	Anticancer agent 69 (Compound 34) is an effective selective anticancer agent with selective inhibition on human prostate cancer cell line PC3 (IC50=26 nM). Anticancer agent 69 can increase ROS level and down-regulate EGF...
T35940	Darinaparsin	Dimethylarsinic glutathione,Darinaparsin
	Darinaparsin is a dimethylated arsenic linked to glutathione. It is cytotoxic to DU145, LNCaP, and PC3 prostate cancer cells (IC50s = 5-10 &#181M) and patient-derived primary prostate cancer cells (IC50s = 2.5-20 &#181M)...
T74126	PROTAC BRD4 Degrader-14
	PROTAC BRD4 Degrader-14, a PROTAC (Proteolysis Targeting Chimera) linked by ligands to von Hippel-Lindau and BRD4, exhibits IC50 values of 1.8 nM and 1.7 nM for BRD4 BD1 and BD2, respectively. This compound effectively d...
T74300	MS143
	MS143, a potent AKT degrader (DC50=46 nM and GI50=0.8 µM in PC3 cells), effectively induces AKT degradation through the ubiquitin-proteasome system in both a concentration- and time-dependent manner, leading to the suppr...
T35629	ATRA-BA Hybrid
	ATRA-BA hybrid is a mutual prodrug form of all-transretinoic acid and butyric acid .1ATRA-BA hybrid is cleaved to release ATRA and BA in isolated mouse plasma. It inhibits the growth of MDA-MB-231 breast and PC3 prostate...
T79202	Anticancer agent 118
	Anticancer Agent 118, an N‑acylated ciprofloxacin derivative, exhibits antibacterial efficacy against Gram-positive strains and antiproliferative effects on prostate PC3 cells, making it a potential candidate for antitum...
T74125	PROTAC BRD4 Degrader-12
	PROTAC BRD4 Degrader-12 (compound 9c) is a PROTAC that links von Hippel-Lindau and BRD4 ligands. When conjugated with STEAP1 and CLL1 antibodies, this compound effectively degrades BRD4 protein in PC3 prostate cancer cel...
T40072	PROTAC BRD4 Degrader-9	PROTAC BRD4 Degrader-9
	PROTAC BRD4 Degrader-9 (compound 8a) is a novel chemical compound consisting of ligands for von Hippel-Lindau and BRD4, connected by a PROTAC moiety. This compound can effectively degrade the BRD4 protein in PC3 prostate...
T70792	SPR519
	SPR519 is a potent dual inhibitor of PI3Kα and mTOR kinases with IC50 (PI3Kalpha) = 30 nM and IC50 (mTOR) = 10 nM. SPR519 exhibits an EC50 of low sub-micromolar range among various tested cancer cell lines such as A2780...
T78980	Pim-1 kinase inhibitor 5		Pim
	Pim-1 kinase inhibitor 5 (Compound 4c), with an IC50 of 0.61 μM, exhibits cytotoxicity against various cancer cell lines, including HepG2, MCF-7, PC3, and HCT-116, with IC50 values ranging from 6.95 to 20.19 μM [1].		Pim
T82089	ICMT-IN-53
	ICMT-IN-53 (compound 12) is an ICMT inhibitor exhibiting an IC50 of 0.96 μM, alongside favorable PAMPA permeability and antiproliferative properties. It demonstrates efficacy by inhibiting the proliferation of MDA-MB-231...
T35561	MS351
	MS351 is an antagonist of chromobox 7 (CBX7) that acts by binding the CBX7 chromodomain. It enhances the binding of long noncoding RNA to the CBX7 chromodomain when used at 25 μM. MS351 induces transcriptional derepressi...
T40073	PROTAC BRD4 Degrader-10	PROTAC BRD4 Degrader-10
	PROTAC BRD4 Degrader-10, also known as compound 8b, is a dual ligand-based PROTAC that combines ligands for von Hippel-Lindau and BRD4. To degrade the BRD4 protein in PC3 prostate cancer cells, PROTAC BRD4 Degrader-10 ca...
T40074	PROTAC BRD4 Degrader-15	PROTAC BRD4 Degrader-15
	PROTAC BRD4 Degrader-15 is a chemical compound consisting of a PROteolysis TArgeting Chimera (PROTAC) linked to ligands specific to von Hippel-Lindau and BRD4. It exhibits an IC50 of 7.2 nM for BRD4 BD1 and 8.1 nM for BR...
T74124	PROTAC BRD4 Degrader-11
	PROTAC BRD4 Degrader-11 (compound 9a), a PROTAC linked through ligands to von Hippel-Lindau and BRD4, effectively targets and degrades the BRD4 protein in PC3 prostate cancer cells when conjugated with STEAP1 and CLL1 an...
TP1895	KYL peptide	KYL
	KYL peptide is an EphA4 receptor tyrosine kinase inhibitor (Kd = 0.8 μM); inhibits EphA4-EphrinA5 interactions (IC50 = 6.34 μM). Prevents AβO induced synaptic damage, dendritic spine loss and prevents the blocking of LTP...
T62278	Anticancer agent 36
	Anticancer agent 36 (compound 11) is a potent anti-microbial and anti-cancer agent, a sulfonylurea derivative. anticancer agent 36 inhibits the microbial growth of Bacillus mycoides, Escherichia coli and Candida albicans...
T63947	GRPR antagonist-1
	GRPR antagonist-1 is a potent antagonist of the gastrin-releasing peptide receptor (GRPR) and is cytotoxic to certain cancer cells (able to act on PC3 cells (IC50: 4.97 μM), Pan02 cells (IC50: 4.36 μM), HGC-27 cells (IC5...
T62754	Anticancer agent 34
	Anticancer agent 34 (compound 9) is a sulfonylurea derivative and a potent anti-microbial and anti-cancer agent. anticancer agent 34 showed inhibition of microbial growth of Mycobacterium, Escherichia coli and Candida al...
T15205	EL-102	EL102	Microtubule Associated , HIF
	EL-102 is a HIF1α inhibitor with anticancer activity that inhibits microtubule protein polymerization and can be used to study prostate cancer.		Microtubule Associated , HIF
T40075	PROTAC BRD4 Degrader-13	PROTAC BRD4 Degrader-13
	PROTAC BRD4 Degrader-13 (compound 9d) is a bioactive compound that functions as a proteolysis targeting chimera (PROTAC), linking ligands for von Hippel-Lindau and BRD4 proteins. In the context of PC3 prostate cancer cel...
T73125	SMTIN-T140		HSP
	SMTIN-T140 (compound 6a), a potent TRAP1 (tumor-necrosis-factor-receptor associated protein 1) inhibitor with an IC50 of 1.646 μM, exhibits anticancer activity by inducing mitochondrial dysfunction, elevating mitochondri...		HSP
T15362	FX-11	LDHA Inhibitor FX11	Dehydrogenase
	FX-11 (LDHA Inhibitor FX11) is A potent, selective and competitive specific inhibitor of lactate dehydrogenase A (LDHA) with a Ki of 8 μM. FX-11 can activate PKM2 (pyruvate kinase M2). FX-11 can reduce ATP levels, induce...		Dehydrogenase

Compounds

SK33

T12928

Synonym:

Target: Androgen Receptor

Abacavir

T1267

Synonym: Epzicom,Ziagen,Abacavir sulfate

Target: Apoptosis, HIV Protease, Reverse Transcriptase

Dasatinib

T1448

Synonym: BMS-354825

Target: Apoptosis, Bcr-Abl, Src, c-Kit, Autophagy

RHPS4

T6967

Synonym: RHPS 4 methosulfate,NSC714187

Target: Apoptosis, Telomerase

Abacavir sulfate

T6367

Synonym: Abacavir Hemisulfate,1592U89,ABC sulfate,Ziagen

Target: Apoptosis, HIV Protease, Reverse Transcriptase

Dasatinib monohydrate

T1448L

Synonym: BMS-354825 Monohydrate

Target: Apoptosis, Bcr-Abl, Src, c-Kit, Ephrin Receptor, Autophagy

Synonym: VPC-32183,VPC 32183

Synonym: VPC 32179,VPC-32179

Target: Fatty Acid Synthase

KYL acetate(676657-00-4 free base)

TP1895L1

Synonym:

Target: Ephrin Receptor

VPC-13163

T29110

Synonym: 2,3-dihydro-2,3'-Bi-1H-indole,VPC13163,NSC52361,NSC 52361,VPC 13163

Target: Others

SMI-16a

T3989

Synonym: PIM1/2 Kinase Inhibitor VI

Target: Others, Fatty Acid Synthase

PROTAC BRD4 Degrader-8

T36628

Synonym: PROTAC BRD4 Degrader-8

Target:

Cysteine protease inhibitor-2

T10924

Synonym:

Target: Cysteine Protease

Synonym: Dimethylarsinic glutathione,Darinaparsin

Target:

PROTAC BRD4 Degrader-14

PROTAC BRD4 Degrader-12

T74125

Synonym:

Target:

PROTAC BRD4 Degrader-9

T40072

Synonym: PROTAC BRD4 Degrader-9

Pim-1 kinase inhibitor 5

PROTAC BRD4 Degrader-10

T40073

Synonym: PROTAC BRD4 Degrader-10

Target:

PROTAC BRD4 Degrader-15

T40074

Synonym: PROTAC BRD4 Degrader-15

Target:

PROTAC BRD4 Degrader-11

Target: Microtubule Associated, HIF

PROTAC BRD4 Degrader-13

T40075

Synonym: PROTAC BRD4 Degrader-13

Synonym: LDHA Inhibitor FX11

Target: Dehydrogenase

Cat No.	Product Name	Targets
T8188	Podophyllotoxone	Others , Microtubule Associated
	Podophyllotoxinone, a natural compound found in Dysosma versipellis, shows inhibitory activity against L1210 leukemia and KB cells in vitro.	Others , Microtubule Associated
TN2054	Periplocymarin	Calcium Channel
	Periplocymarin is a cardiac glycoside with anticancer potential isolated from Periploca sepium and Periploca graeca.	Calcium Channel
TN1198	19-Hydroxybufalin	Others
	19-Hydroxybufalin is a natural product, inhibits epithelial-mesenchymal transition and attenuates the migration and invasion of PC3 cells.	Others
TN6638	(E)-6-O-(p-coumaroyl)scandoside methyl ester
	(E)-6-O-(p-coumaroyl)scandoside methyl ester shows moderate anti-proliferation effect on PC3 human androgen-independent prostate cancer cells.
TN3113	5-Heptadecylresorcinol	Others
	5-Heptadecylresorcinol has strong inhibitory property against the growth of PC3 cells.	Others
T36489	Malformin A
	Malformin A is a cyclopentapeptide fungal metabolite that has been found in A. niger and has diverse biological activities. It is a plant growth regulator that induces malformations in plant structure. Malformin A inhib...
TN6059	Demethoxyfumitremorgin C
	Demethoxyfumitremorgin C and tryprostatin B are fungal inhibitors of mammalian cell cycle progression at the G(2)/M transition. Demethoxyfumitremorgin C inhibits the proliferation of PC3 human prostate cancer cells via t...
T37442	Aspergillin PZ
	Aspergillin PZ is a fungal metabolite originally isolated from A. awamori. It induces morphological deformation of P. oryzae conidia when used at a concentration of 89 nM. Aspergillin PZ is active against S. epidermidis ...
T37452	Stephacidin B
	Stephacidin B is a fungal metabolite that has been found inA. ochraceus.1Dimeric stephacidin B is rapidly converted to a monomer, avrainvillamide ,in vitro.2Stephacidin B is cytotoxic to a variety of cancer cells, includ...
T36749	Herboxidiene
	Herboxidiene is a polyketide originally isolated from S. chromofuscus that has diverse biological activities.[1],[2,][3],[4],[5] It inhibits growth of HeLa S3, SK-MEL-2, PC3, A549, and EBC-1 cells with GI50 values rangin...

Natural Products

Podophyllotoxone

T8188

Synonym:

Target: Others, Microtubule Associated

Periplocymarin

TN2054

Synonym:

Target: Calcium Channel

(E)-6-O-(p-coumaroyl)scandoside methyl ester

TN6638

Synonym:

Target:

5-Heptadecylresorcinol

Demethoxyfumitremorgin C

Recombinant Proteins

Species：

Expression System：

Tag：

Cat No.	Product Name	Species	Expression System
TMPK-00630	PSMP Protein, Mouse, Recombinant (hFc)	Mouse	HEK293 Cells
	PSMP Protein, Mouse, Recombinant (hFc) is expressed in HEK293 mammalian cells with C-hFc tag. The predicted molecular weight is 37.9 kDa and the accession number is B1AWI6.
TMPK-00981	PSMP Protein, Human, Recombinant (hFc)	Human	HEK293 Cells
	PSMP Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with C-hFc tag. The predicted molecular weight is 37.9 kDa and the accession number is Q1L6U9.
TMPH-01090	CBX8 Protein, Human, Recombinant (His)	Human	E. coli
	Component of a Polycomb group (PcG) multiprotein PRC1-like complex, a complex class required to maintain the transcriptionally repressive state of many genes, including Hox genes, throughout development. PcG PRC1 complex...
TMPY-01635	PCSK1 Protein, Human, Recombinant (His)	Human	HEK293 Cells
	Neuroendocrine convertase 1, also known as Prohormone convertase 1, Proprotein convertase 1, PCSK1 and NEC1, is an enzyme which belongs to the peptidase S8 family and Furin subfamily. PCSK1 is an enzyme that performs the...
TMPJ-01354	ATG3 Protein, Human, Recombinant	Human	E. coli
	Ubiquitin-like-conjugating enzyme ATG3 (ATG3), also known as Apg3L and Apg3p, functions as a regulatory component of autophagosome biogenesis necessary for autophagy. ATG3 exhibits 98% aa sequence identity with both its ...
TMPY-00502	Glypican 3/GPC3 Protein, Mouse, Recombinant (His)	Mouse	Baculovirus Insect Cells
	Glypican 3/GPC3 Protein, Mouse, Recombinant (His) is expressed in Baculovirus insect cells with His tag. The predicted molecular weight is 62 kDa and the accession number is Q3TWB2.
TMPY-01283	Glypican 3/GPC3 Protein, Human, Recombinant (His)	Human	HEK293 Cells
	Glypican 3/GPC3 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 62 kDa and the accession number is P51654-1.
TMPK-00336	GPC3 Protein-VLP, Human, Recombinant	Human	E. coli
	Glypican-3 is a protein ,which is encoded by the GPC3 gene in humans.The protein core of GPC3 consists of two subunits, where the N-terminal subunit has a size of ~40 kDa and the C-terminal subunit is ~30 kDa.Glypican 3 ...
TMPY-05805	Glypican 3/GPC3 Protein, Human, Recombinant (S495A, hFc)	Human	HEK293 Cells
	Glypican 3/GPC3 Protein, Human, Recombinant (S495A, hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 86.46 kDa and the accession number is I6QTG3.
TMPY-05106	Glypican 3/GPC3 Protein, Human, Recombinant (His), Biotinylated	Human	HEK293 Cells
	Glypican 3/GPC3 Protein, Human, Recombinant (His), Biotinylated is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 62.2 kDa and the accession number is P51654-1.
TMPY-05806	Glypican 3/GPC3 Protein, Human, Recombinant (S495A, mFc)	Human	HEK293 Cells
	Glypican 3/GPC3 Protein, Human, Recombinant (S495A, mFc) is expressed in HEK293 mammalian cells with mFc tag. The predicted molecular weight is 86.11 kDa and the accession number is I6QTG3.
TMPJ-01423	GPC3 Protein, Rhesus macaque, Recombinant (His)	Rhesus	HEK293 Cells
	GPC3 Protein, Rhesus macaque, Recombinant (His) is expressed in HEK293 mammalian cells with C-6xHis tag. The predicted molecular weight is 38 and 65-120 KDa and the accession number is XP_005594665.1.
TMPY-06820	Glypican 3/GPC3 Protein, Cynomolgus, Recombinant (His)	Cynomolgus	HEK293 Cells
	Glypican 3/GPC3 Protein, Cynomolgus, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 61.64 kDa and the accession number is XP_005594665.1.
TMPH-01730	MYBPC3 Protein, Human, Recombinant (His & SUMO)	Human	E. coli
	Thick filament-associated protein located in the crossbridge region of vertebrate striated muscle a bands. In vitro it binds MHC, F-actin and native thin filaments, and modifies the activity of actin-activated myosin ATP...
TMPJ-00337	GPC3 Protein, Human, Recombinant (His & Avi), Biotinylated	Human	HEK293 Cells
	GPC3 Protein, Human, Recombinant (His & Avi), Biotinylated is expressed in HEK293 mammalian cells with C-6xHis-Avi tag. The predicted molecular weight is 60-180 and 36-44 KDa and the accession number is P51654.
TMPH-03307	Glypican 3/GPC3 Protein, Rat, Recombinant (His)	Rat	P. pastoris (Yeast)
	Glypican 3/GPC3 Protein, Rat, Recombinant (His) is expressed in Yeast.
TMPK-00337	GPC3 Protein-VLP, Human, Recombinant (aa 438-554)	Human	HEK293 Cells
	Glypican-3 is a protein ,which is encoded by the GPC3 gene in humans.The protein core of GPC3 consists of two subunits, where the N-terminal subunit has a size of ~40 kDa and the C-terminal subunit is ~30 kDa.Glypican 3 ...
TMPY-06751	Glypican 3/GPC3 Protein, Canine, Recombinant (His)	Canine	HEK293 Cells
	Glypican 3/GPC3 Protein, Canine, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 62.07 kDa and the accession number is A0A8C0TMC5.
TMPY-06877	Glypican 3/GPC3 Protein, Human, Recombinant (His & Avi), Biotinylated	Human	HEK293 Cells
	Glypican 3/GPC3 Protein, Human, Recombinant (His & Avi), Biotinylated is expressed in HEK293 mammalian cells with His and Avi tag. The predicted molecular weight is 64.05 kDa and the accession number is P51654-1.
TMPY-02122	IFNGR2 Protein, Mouse, Recombinant (His)	Mouse	HEK293 Cells
	Interferon-gamma receptor beta chain (IFNgammaR2), also known as IFNGR2, belongs to the type II cytokine receptor family, whose deficiency is a cause of autosomal recessive mendelian susceptibility to mycobacterial disea...