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Cat No. | Product Name | Synonyms | Targets |
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T30344 | Benzamide, N-(8-(p-aminophenoxy)octyl)- | ||
Benzamide, N-(8-(p-aminophenoxy)octyl)- is a bioactive chemical. | |||
T30068 | Aniline, N-methyl-p-(8-phenoxyoctyloxy)- | ||
Aniline, N-methyl-p-(8-phenoxyoctyloxy)- is a Drug / Therapeutic Agent. | |||
TP2389 | Laminin B1 octapeptide P-8 | Asp-pro-gln-tyr-ile-gln-ser-arg,Dpgyigsr | |
Laminin B1 octapeptide P-8 is a synthetic laminin B1 chain octapeptide with laminin receptor binding ability. | |||
TP1931L1 | [D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P acetate | [D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P acetate(96736-12-8 free base) | cholecystokinin |
[D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P acetate ([D-Arg1,D-Phe5,D-Trp7,9,Leu11]-Substance P acetate (96736-12-8 free base)) is a broad spectrum neuropeptide inverse agonist and antagonist. Potent full inverse agonist ... | |||
TP2103L | [D-p-Cl-Phe6,Leu17]-VIP acetate | Others | |
[D-p-Cl-Phe6,Leu17]-VIP acetate is a competitive and selective antagonist of vasoactive intestinal peptide (VIP) receptor (IC50 = 125.8 nM). | |||
T40685L | Orphan GPCR SP9155 agonist P550 (mouse, rat) acetate | Orphan GPCR SP9155 agonist P550 (mouse, rat) acetate (600171-70-8 Free base) | Others |
Orphan GPCR SP9155 agonist P550 (mouse, rat) acetate (Orphan GPCR SP9155 agonist P550 ) is a member of the RFamide peptide family with orexigenic effects. | |||
T0089 | Cetirizine dihydrochloride | P071,UCB P071,Cetirizine DiHCl | Histamine Receptor |
Cetirizine dihydrochloride (UCB P071) is an effective second-generation histamine H1 antagonist that is potent in the therapy of allergic rhinitis, confirmed urticaria, and pollen-induced asthma. Unlike other conventiona... | |||
TP1549L | NY-BR-1 p904 A2 acetate(347142-73-8 free base) | Others | |
T-cell clones specific for this NY-BR-1 p904 A2 acetate(347142-73-8 free base) can recognize breast tumor cells expressing NY-BR-1. | |||
T124022 | 8-p-Coumaroylharpagide | ||
T9150 | SCR130 | 1,7,9-Triazaspiro[4.5]dec-1-ene-6,10-dione, 2,4-bis(4-chlorophenyl)-8-thioxo- | Apoptosis , Others , DNA/RNA Synthesis |
SCR130 (1,7,9-Triazaspiro[4.5]dec-1-ene-6,10-dione, 2,4-bis(4-chlorophenyl)-8-thioxo-) is enzyme inhibition, antiproliferative effects and antifungal activity. | |||
T5962 | TRPM8 antagonist WS-3 | Cyclohexanecarboxamide,N-Ethyl-p-menthane-3-carboxamide,N-Ethyl-2-isopropyl-5-methylcyclohexanecarboxamide | TRP/TRPV Channel |
TRPM8 antagonist WS-3 (Cyclohexanecarboxamide) is an agonist of TRPM8( EC50 : 3.7 μM). | |||
T39826 | CBP/p300-IN-8 | CBP/p300-IN-8 | |
CBP/p300-IN-8 is a potent inhibitor of the CBP/P300 family of bromodomains . CBP/p300-IN-8 inhibits CBP ( IC 50 =0.01-0.1 μΜ) and BRD4 ( IC 50 =1-1000 μΜ) activity. | |||
T11597L | IACS-9571 Hydrochloride (1800477-30-8 free base) | IACS-9571 Hydrochloride,ASIS-P040 Hydrochloride | Epigenetic Reader Domain |
IACS-9571 Hydrochloride is a selective and potent inhibitor of TRIM24 and BRPF1, (IC50: 8 nM for TRIM24; Kds: 31 nM and 14 nM for TRIM24 and BRPF1). | |||
T5952 | Diniconazole | Rac-diniconazole | Antibacterial |
Diniconazole (Rac-diniconazole) is a fungicide. It is known as a plant hormone abscisic acid (ABA) catabolic inhibitor, and acts as a potent competitive inhibitor of recombinant Arabidopsis ABA 8'-hydroxylase, CYP707A3. | |||
T36949 | Niaprazine | 5-HT Receptor , Adrenergic Receptor , Histamine Receptor | |
Niaprazine is a histamine H1-receptor antagonist with marked sedative properties. Niaprazine has antihistamine and antiserotonin activities and can be used for sleep disorder research[1][2]. Niaprazine exhibits a low aff... | |||
T14492 | BAL-30072 | Others | |
BAL30072 shows MIC90 values of 4 μg/mL for MDR Acinetobacter spp. and 8 μg/mL for MDR P. aeruginosa, respectively[1][2]. BAL-30072, a siderophore sulfactam, is a monocyclic beta-lactam antibiotic, with activity against m... | |||
T39958 | (32-Carbonyl)-RMC-5552 | ||
(32-Carbonyl)-RMC-5552 is a highly effective mTOR inhibitor, exhibiting inhibitory effects on both mTORC1 and mTORC2 substrate phosphorylation. Specifically, it significantly suppresses the phosphorylation of p-P70S6K-(T... | |||
T28348 | PD 404182 | PD404182,PD-404182 | |
PD-404182, an inhibitor of KDO 8-P synthase (Ki = 26 nM), is a otential antibiotic of gram negative bacteria. PD-404182 also exhibits antiviral and antiangiogenic activity in vitro. | |||
TNU0199 | 8-Hydroxyadenosine | ||
Nucleoside Derivatives - 8-Modified purine nucleosides; Drugs and Inhibitors; Anticancer antibiotics; oxidized nucleic acid adduct; precursor of phosmidosine (P-prodrug) | |||
T67054 | 1-(P-Toluenesulfonyl)imidazole | ||
1-(P-Toluenesulfonyl)imidazole is a useful organic compound for research related to life sciences. The catalog number is T67054 and the CAS number is 2232-08-8. | |||
T62936 | Antimalarial agent 8 | ||
Antimalarial agent 8 (Compound 7e) is a novel, orally active antimalarial agent that is effective against P. falciparum in vitro and effective orally in an in vivo mouse model of malaria (40 mg/kg). | |||
T65805 | L-Leucine benzyl ester p-toluenesulfonate salt | ||
L-Leucine benzyl ester p-toluenesulfonate salt is a useful organic compound for research related to life sciences. The catalog number is T65805 and the CAS number is 1738-77-8. | |||
T64762 | P(t-Bu)3 Pd G3 | ||
P(t-Bu)3 Pd G3 is a useful organic compound for research related to life sciences. The catalog number is T64762 and the CAS number is 1445086-17-8. | |||
T39672 | Ac-Ile-Glu-Thr-Asp-pNA | ||
Ac-Ile-Glu-Thr-Asp-pNA is a caspase-8 substrate that undergoes enzymatic binding and cleavage specifically at the Ile-Glu-Thr-Asp (IETD) peptide sequence. This cleavage results in the release of p-nitroalinide, which can... | |||
TNU1040 | 3-Deoxy-1,2-O-isopropylidene-5-O-(p-toluoyl)- α-D-glycero-pent-3-enofuranose | ||
3-Deoxy-1,2-O-isopropylidene-5-O-(p-toluoyl)- α-D-glycero-pent-3-enofuranose is a useful organic compound for research related to life sciences. The catalog number is TNU1040 and the CAS number is 75096-63-8. | |||
T74496 | LA-Bac8c | ||
LA-Bac8c, a lipoic acid-modified antimicrobial peptide, exhibits improved antimicrobial efficacy. It effectively inhibits S. aureus, MRSA, S. epidermidis, E. coli, and P. aeruginosa, demonstrating minimum inhibitory conc... | |||
T36076 | Ciprofibrate impurity A | ||
Ciprofibrate impurity A is an impurity of Ciprofibrate. Ciprofibrate is a PPARα agonist[1]. [1]. Passilly, P., et al., Phosphorylation of peroxisome proliferator-activated receptor alpha in rat Fao cells and stimulation ... | |||
T60315 | Anti-infective agent 1 | ||
Anti-infective agent 1 (compound 3a) serves as a potent, selective antiprotozoal and antimycobacterial compound. It showcases antiparasitic efficacy against P. falciparum and T. brucei rhodesiense, demonstrating IC50 val... | |||
T80274 | Lynronne-1 | ||
Lynronne-1, an antimicrobial peptide, exhibits activity against Gram-positive bacteria, including multi-drug resistant (MDR) strains, with a minimal inhibitory concentration (MIC) of 8-32 μg/mL for methicillin-resistant ... | |||
T83826 | 1,2,3,6,7,8-Hexachlorodibenzo-p-dioxin | 1,2,3,6,7,8-HxCDD,PCDD 67 | |
1,2,3,6,7,8-Hexachlorodibenzo-p-dioxin, a polychlorinated dibenzodioxin (PCDD), acts as an agonist for the aryl hydrocarbon receptor (AhR; EC50s = 5.4 and 9.3 nM at 4 and 8 h, respectively, in a reporter assay). It has b... | |||
TP1054 | PACAP (1-38), human, ovine, rat TFA | Pituitary Adenylate Cyclase Activating Polypeptide 38 (TFA) | |
PACAP (1-38), a novel neuropeptide isolated from the bovine hypothalamus is more active than vasoactive intestinal peptide (VIP) in stimulating adenylate cyclase (EC50=7 nM). PACAP 1-38 (10-9 M) increased substance P (SP... | |||
T83735 | Pap12-6 TFA | ||
Pap12-6, an antibacterial peptide originating from the first twelve N-terminal amino acids of papiliocin found in P. xuthus larvae, exhibits activity against a range of eight Gram-negative bacteria (e.g., E. coli, P. aer... | |||
T70507 | KAI-407 | ||
KAI407 is a potent non-8-aminoquinoline compound that kills Plasmodium cynomolgi early dormant liver stage parasites in vitro. KAI407 showed an activity profile similar to that of primaquine (PQ), efficiently killing th... | |||
T36746 | Leoidin | ||
Leoidin is a depsidone originally isolated from L. gangaleoides that has antibacterial and enzyme inhibitory activities.1,2,3 It is active against the bacteria E. faecalis, H. influenzae, M. catarrhalis, S. aureus, and S... | |||
T21633 | N-3-oxo-dodecanoyl-L-Homoserine lactone | ||
N-3-oxo-dodecanoyl-L-Homoserine lactone (3-oxo-C12-HSL), a quorum-sensing signaling molecule, is synthesized by P. aeruginosa and specific B. cepacia complex strains [1][2]. This regulatory mechanism facilitates bacteria... | |||
T37362 | 7α-Thiomethylspironolactone | ||
7α-Thiomethylspironolactone is a major metabolite of the synthetic steroid spironolactone.1,2 1.Jankowski, A., Skorek-Jankowska, A., and Lamparczyk, H.Simultaneous determination of spironolactone and its metabolites in h... | |||
T38215 | 1-Hydroxy-ibuprofen | ||
1-Hydroxy Ibuprofen, a metabolite of Ibuprofen in P. australis[1], functions as an anti-inflammatory inhibitor specifically targeting COX-1 and COX-2, with inhibitory concentration 50 (IC50) values of 13 μM and 370 μM, r... | |||
T14382 | AZD7687 | Others | |
AZD7687 is a potent and selective DGAT1 inhibitor with an IC50 value of 80 nM (hDGAT1). IC50 value: 80 nM [1] Target: DGAT1 in vitro: Plasma AZD7687 exposure was measured repeatedly. AZD7687 markedly reduced postprandial... | |||
T35494 | (±)11(12)-EET | ||
(±)11(12)-EET is a fully racemic version of the R/S enantiomeric forms biosynthesized from arachidonic acid by cytochrome P450 enzymes.[1][2][3[]A higher proportion of 11(R),12(S)-EET is produced by the CYP450 isoforms C... | |||
T83706 | BMAP 28 (bovine) TFA | Cathelicidin-5 (132-158),Bovine Myeloid Antimicrobial Peptide 28 | |
Bovine Myeloid Antimicrobial Peptide (BMAP) 28, a synthetic peptide derived from bovine cathelicidin-5 (amino acids 132-158), exhibits antimicrobial activity against E. coli, S. aureus, MRSA, S. epidermidis, and the fung... | |||
T35671 | Salazinic Acid | ||
Salazinic acid is a depsidone lichen metabolite that has been found in P. sulcata.1 It is active against B. cereus, B. subtilis, S. aureus, P. aeruginosa, S. typhimurium, C. albicans, and A. niger in vitro (MICs = 3.9-30... | |||
T36806 | TPC2-A1-P | TPC2-A1-P | |
TPC2-A1-P is a potent, membrane-permeable agonist of the two-pore channel 2 (TPC2), exhibiting an EC50 of 10.5 μM. It exerts its effects by mimicking the physiological actions of PI(3,5)P2, and demonstrates greater effic... | |||
T36648 | Tucatinib hemiethanolate | ||
Tucatinib (Irbinitinib) hemiethanolate is a potent, orally active and selective HER2 inhibitor with an IC50 of 8 nM. Tucatinib hemiethanolate has nanomolar activity against purified HER2 enzyme and is approximately 500-f... | |||
T36629 | Givinostat | ||
Givinostat (ITF-2357) is a HDAC inhibitor with an IC50 of 198 and 157 nM for HDAC1 and HDAC3, respectively. Givinostat (ITF2357) suppresses total LPS-induced IL-1β production robustly compared with the reduction by ITF30... | |||
T35829 | CC-90005 | ||
CC-90005 is a potent, selective and orally active inhibitor of protein kinase C-θ (PKC-θ), with an IC50 of 8 nM. CC-90005 shows selectivity for PKC-θ over PKC-δ (IC50=4440 nM). CC-90005 can inhibit T cell activation by I... | |||
T35840 | 4-Amino-6-chloro-1,3-benzenedisulfonamide | ||
4-Amino-6-chloro-1,3-benzenedisulfonamide is a carbonic anhydrase inhibitor.1 Formulations containing this compound are diuretics.2 4-Amino-6-chloro-1,3-benzenedisulfonamide is detected as a hydrolysis product of chlorot... | |||
T35757 | Beauvericin A | ||
Beauvericin A is a cyclodepsipeptide and derivative of beauvericin originally isolated fromB. bassianathat has diverse biological activities.1,2,3It is active againstM. tuberculosis(MIC = 25 μg/ml) andP. falciparum(IC50=... | |||
T36521 | Alaproclate (hydrochloride) | ||
Alaproclate is a selective serotonin reuptake inhibitor (SSRI).1,2 It inhibits depletion of serotonin (5-HT) induced by 4-methyl-α-ethyl-m-tyramine in rat cerebral cortex, hippocampus, hypothalamus, and striatum (EC50s =... | |||
T37761 | Fura-FF (potassium salt) | ||
Fura-FF is a difluorinated derivative of the calcium indicator fura-2. Unlike, fura-2, fura-FF has negligible magnesium sensitivity, thus reducing interference from this cation.[1] Fura-FF also has a higher calcium disso... | |||
T36215 | 17R(18S)-EpETE | ||
17R(18S)-EpETE is an oxylipin and a cytochrome P450 metabolite of eicosapentaenoic acid .1,217R(18S)-EpETE is an activator of large-conductance calcium-activated potassium (BKCa) channels, increasing the potassium curren... |
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
TN4729 | p-Menth-8-ene-1,2-diol | Others | |
p-Menth-8-ene-1,2-diol is a natural product for research related to life sciences. The catalog number is TN4729 and the CAS number is 57457-97-3. | |||
TN5868 | 8-Hydroxythymol | p-Cymene-3,8-diol | |
8-Hydroxythymol is a natural product for research related to life sciences. The catalog number is TN5868 and the CAS number is 4478-33-5. | |||
TN1343 | 8-Geranyloxypsoralen | Anti-infection , P450 , BACE | |
8-Geranyloxypsoralen inhibits α2-secretase (BACE1) activity in non-competitive manner, with the IC(50) values <25.0 μM, it can induce vasorelaxation on rat arterial tissues. 8-Geranyloxypsoralen possesses nematicidal act... | |||
T13617 | Cis-p-Menthan-1,8-diol | 4-p-Menthan-1,8-diol | Others |
cis- p- Menthan- 1, 8- diol is a natural menthane monoterpenoid. | |||
TN5238 | Viscidulin II | IL Receptor , TNF | |
Viscidulin II can be potential therapeutic agents against P. acnes-induced skin inflammation, it can significantly suppress P. acnes-induced IL-8 and IL-1β production in THP-1 cells, concomitant intradermal injection of ... | |||
TN3494 | Benzoylgomisin P | Others | |
Benzoylgomisin P is a natural product for research related to life sciences. The catalog number is TN3494 and the CAS number is 129445-43-8. | |||
TN5729 | Giffonin P | ||
Giffonin P is a natural product for research related to life sciences. The catalog number is TN5729 and the CAS number is 1830306-93-8. | |||
TN5833 | 6-O-(p-Hydroxybenzoyl)glucose | ||
6-O-(p-Hydroxybenzoyl)glucose is a natural product for research related to life sciences. The catalog number is TN5833 and the CAS number is 202337-44-8. | |||
TN5971 | 16-Oxolyclanitin-29-yl p-coumarate | ||
16-Oxolyclanitin-29-yl p-coumarate is a natural product for research related to life sciences. The catalog number is TN5971 and the CAS number is 140701-70-8. | |||
TN6287 | Apigenin 7-O-(2'',6''-di-O-E-p-coumaroyl)glucoside | Anisofolin B | |
Apigenin 7-O-(2'',6''-di-O-E-p-coumaroyl)glucoside is a natural product for research related to life sciences. The catalog number is TN6287 and the CAS number is 1448779-19-8. | |||
TN6304 | Apigenin 4'-O-(2'',6''-di-O-E-p-coumaroyl)glucoside | ||
Apigenin 4'-O-(2'',6''-di-O-E-p-coumaroyl)glucoside is a natural product for research related to life sciences. The catalog number is TN6304 and the CAS number is 71781-79-8. | |||
TN3292 | 8-Prenyldaidzein | Others | |
8-Prenyldaidzein has cytotoxic properties against P-388 cells, its IC 50 values 5.82 ug/mL, it also exhibits very high antioxidant activity against DPPH radical scavenging. | |||
T40859 | 5-Hydroxy-8-methoxypsoralen | 5-Hydroxyxanthotoxin,5-Hydroxy-8-methoxypsoralen | |
5-Hydroxy-8-methoxypsoralen (5-Hydroxyxanthotoxin) is a metabolite derived from Xanthotoxin, which acts as a potent tricyclic furocoumarin suicide inhibitor of CYP (cytochrome P-450). It is employed as an agent for the t... | |||
T38015 | Herquline A | ||
Herquline A is an alkaloid fungal metabolite originally isolated from P. herquei. It inhibits cell death induced by influenza A strain A/PR/8/34 in MDCK cells with an IC50 value of 10 μg/ml and inhibits viral replication... | |||
T38262 | Sphingosine (d14:1) | ||
Sphingosine (d14:1) is a bioactive sphingolipid that has been found in B. mori (silkworm), P. clarkii (crayfish), and A. aurita (jellyfish) extracts. It increases the germination rate of N. rileyi, an entomopathogenic fu... | |||
T35754 | Aszonapyrone A | ||
Aszonapyrone A is a meroditerpene fungal metabolite that has been found in Neosartorya and has diverse biological activities.1,2,3 It inhibits the growth of MCF-7, NCI H460, and A375-C5 cancer cells (GI50s = 13.6, 11.6, ... | |||
T36329 | Terpendole I | ||
Terpendole I is a fungal metabolite that has been found in A. yamanashiensis.1 It is a weak inhibitor of acyl-coenzyme A:cholesterol acyltransferase (ACAT; IC50 = 145 μM) and is active against the bacteria B. cereus and ... | |||
T36000 | 3-Hydroxyterphenyllin | ||
3-Hydroxyterphenyllin is a p-terphenyl fungal metabolite originally isolated from A. candidus that has diverse biological activities, including antioxidant, antiproliferative, antibacterial, and antiviral properties.1,2,... | |||
T35750 | Trypacidin | ||
Trypacidin is a fungal metabolite originally isolated fromA. fumigatus.1It is active againstB. subtilisandM. bovis(MICs = 12.5 and 1.25 μg/ml, respectively), as well asT. cruziandT. gondii(MICs = 5-10 and 10-20 μg/ml, re... |
Cat No. | Product Name | Species | Expression System |
---|---|---|---|
TMPY-01356 | S100A8 Protein, Human, Recombinant (His) | Human | Baculovirus Insect Cells |
S100A8 Protein, Human, Recombinant (His) is expressed in Baculovirus insect cells with His tag. The predicted molecular weight is 12.2 kDa and the accession number is P05109. | |||
TMPY-02215 | Coagulation factor IX/F9 Protein, Human, Recombinant (His) | Human | HEK293 Cells |
Coagulation factor IX/F9 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 50 kDa and the accession number is AAB59620.1. | |||
TMPY-01563 | PMP2 Protein, Human, Recombinant (His) | Human | E. coli |
Myelin P2 protein, also known as PMP2, is a cytosolic protein found primarily in peripheral nerves. It Belongs to the calycin superfamily. Fatty-acid binding protein (FABP) family. PMP2 is a small, basic, and cytoplasmic... | |||
TMPY-05355 | Coagulation factor IX/F9 Protein, Human, Recombinant (hFc) | Human | HEK293 Cells |
Coagulation factor IX/F9 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 75.5 kDa and the accession number is P00740-1. | |||
TMPH-03625 | Alpha-mammal toxin Ts2 Protein, Tityus serrulatus, Recombinant (His & Myc) | Tityus serrulatus | Baculovirus Insect Cells |
Alpha-mammal toxin Ts2 Protein, Tityus serrulatus, Recombinant (His & Myc) is expressed in Baculovirus insect cells with N-10xHis and C-Myc tag. The predicted molecular weight is 10.9 kDa and the accession number is P684... | |||
TMPH-01186 | CYP2C9 Protein, Human, Recombinant (His & Myc) | Human | E. coli |
CYP2C9 Protein, Human, Recombinant (His & Myc) is expressed in E. coli. | |||
TMPY-06668 | Act d 8 Protein, Actinidia deliciosa, Recombinant | Actinidia deliciosa | P. pastoris (Yeast) |
Act d 8 Protein, Actinidia deliciosa, Recombinant is expressed in P. pastoris yeast expression system. The predicted molecular weight is 26.7 kDa. | |||
TMPY-06676 | Cor a 8 Protein, Corylus avellana, Recombinant | Corylus avellana | P. pastoris (Yeast) |
Cor a 8 Protein, Corylus avellana, Recombinant is expressed in P. pastoris yeast expression system. The predicted molecular weight is 9 kDa. | |||
TMPH-02295 | UAP1 Protein, Human, Recombinant (His) | Human | P. pastoris (Yeast) |
Converts UTP and GlcNAc-1-P into UDP-GlcNAc, and UTP and GalNAc-1-P into UDP-GalNAc. Isoform AGX1 has 2 to 3 times higher activity towards GalNAc-1-P, while isoform AGX2 has 8 times more activity towards GlcNAc-1-P. | |||
TMPH-02294 | UAP1 Protein, Human, Recombinant (E. coli, His) | Human | E. coli |
Converts UTP and GlcNAc-1-P into UDP-GlcNAc, and UTP and GalNAc-1-P into UDP-GalNAc. Isoform AGX1 has 2 to 3 times higher activity towards GalNAc-1-P, while isoform AGX2 has 8 times more activity towards GlcNAc-1-P. | |||
TMPY-04123 | CEACAM1 Protein, Human, Recombinant (His & hFc) | Human | HEK293 Cells |
CEACAM1 Protein, Human, Recombinant (His & hFc) is expressed in HEK293 mammalian cells with His and hFc tag. The predicted molecular weight is 71.4 kDa and the accession number is P13688-8. | |||
TMPY-00668 | APP/Protease nexin-II Protein, Human, Recombinant (hFc) | Human | HEK293 Cells |
APP/Protease nexin-II Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with hFc tag. The predicted molecular weight is 101 kDa and the accession number is P05067-8. | |||
TMPY-06707 | Mucin-1/MUC1 Protein, Human, Recombinant (aa 1-173, His) | Human | HEK293 Cells |
Mucin-1/MUC1 Protein, Human, Recombinant (aa 1-173, His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 17.49 kDa and the accession number is P15941-8. | |||
TMPJ-00828 | Tau-F Protein, Human, Recombinant | Human | E. coli |
Tau proteins are proteins which contain four Tau/MAP repeats. They promote microtubule assembly and stability, and might be involved in the establishment and maintenance of neuronal polarity. They are abundant in neurons... | |||
TMPJ-00808 | CD45RA Protein, Human, Recombinant (His) | Human | HEK293 Cells |
CD45RA Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with C-6xHis tag. The predicted molecular weight is 100-135 KDa and the accession number is P08575-8. | |||
TMPJ-01330 | CD299 Protein, Human, Recombinant (His & Flag) | Human | HEK293 Cells |
CD299 is also known as DC-SIGNR and CLEC4M, is a type II integral membrane protein. DC-SIGNR exists as a homotetramer, and the tandem repeat domain, also called neck domain, mediates oligermerization. Multiple human DC-S... | |||
TMPH-01705 | Mucin-1/MUC1 Protein, Human, Recombinant (His) | Human | E. coli |
Mucin-1/MUC1 Protein, Human, Recombinant (His) is expressed in E. coli expression system with N-6xHis tag. The predicted molecular weight is 31.2 kDa and the accession number is P15941-8. | |||
TMPY-00717 | CEACAM1 Protein, Human, Recombinant (His) | Human | HEK293 Cells |
CEACAM1 Protein, Human, Recombinant (His) is expressed in HEK293 mammalian cells with His tag. The predicted molecular weight is 44.8 kDa and the accession number is P13688-8. |