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PCI-34051 5MG - GBM-3396-5MG

ASUNAPREVIR 5MG - GBM-4928-5MG

MLS-544460 5MG - GBM-5332-5MG

AZD1208 5MG - GBM-4781-5MG

DEXRAZOXANE 10MG - GBM-2606-10MG

COMPOUND E 1MG - GBM-3479-1MG

AS1842856 25MG - GBM-5344-25MG

TALABOSTAT MESYLATE 25MG - GBM-4005-25MG

VINPOCETINE 50MG - GBM-1126-50MG

ML133 HCL 25MG - GBM-5098-25MG

FB23-2 25MG - GBM-4852-25MG

DEXRAZOXANE 50MG - GBM-2606-50MG

ICRF-193 5MG - GBM-5056-5MG

AZD7648 25MG - GBM-4108-25MG

ASCOCHLORIN 100UG - GBM-5296-100UG

SORAFENIB TOSYLATE 50MG - GBM-3690-50MG

FB23-2 5MG - GBM-4852-5MG

SP100030 5MG - GBM-3996-5MG

ASCOCHLORIN 500UG - GBM-5296-500UG

BLEBBISTATIN 5MG - GBM-2832-5MG

P505-15 5MG - GBM-4650-5MG

TGX-221 5MG - GBM-4783-5MG

ANLE138B 10MG - GBM-4945-10MG

P505-15 25MG - GBM-4650-25MG

ILICICOLIN H 100UG - GBM-3243-100UG

LINOLEOYL GLYCINE 25MG - GBM-5516-25MG

MLS-544460 25MG - GBM-5332-25MG

MARIMASTAT 1MG - GBM-5445-1MG

LY364947 25MG - GBM-1492-25MG

BAKUCHIOL 10MG - GBM-3161-10MG

COMPOUND E 5MG - GBM-3479-5MG

XL413·HCL 25MG - GBM-4414-25MG

ROCAGLAMIDE 2MG - GBM-2484-2MG

IFSP1 25MG - GBM-5043-25MG

TGX-221 25MG - GBM-4783-25MG

KONINGIC ACID (KA) 200UG - GBM-3326-200UG

CEDIRANIB 25MG - GBM-5757-25MG

17-AAG 25MG - GBM-1097-25MG

EFT508 25MG - GBM-4081-25MG

PLERIXAFOR 25MG - GBM-2864-25MG

VORASIDENIB 25MG - GBM-4659-25MG

AZD1208 25MG - GBM-4781-25MG

MARIMASTAT 5MG - GBM-5445-5MG

PROTEIN ARGININE INHIBITR 50UG - 539209-5MG

CHK2 INHIBITOR-500UG - 220485-500UG

Protease Inhibitor Cocktail Set III, Animal-Free - 535140-1SET, 1 set, Protease inhibitor cocktail

Protease Inhibitor Cocktail Set III, Animal-Free - 535140-1ML, 1 mL. 1 ml, Protease Inhibitor Cocktail. Protease inhibitor cocktail

PROTEASE INHIBITOR COCKTAIL SE - 539136-1ML

Protease Inhibitor Cocktail Set I, Animal-Free, Calbiochem®, MilliporeSigma - 535142-1ML, 1 mL, Protease Inhibitor Cocktail Set I, Animal-Free

Protease Inhibitor Cocktail Set I, Animal-Free, Calbiochem®, MilliporeSigma - 535142-1SET, 1 Set, Protease Inhibitor Cocktail Set I, Animal-Free

PROTEASE INHIBITOR COCKTAIL 1M - 535141-1ML

PROTEASE INHIBITOR COCKTAIL SE - 535141-1SET

PIFITHRIN-ALPHA NITRIC 5MG. 5MG

SIRT 1/2 INHIBITOR IV CAMBINOL. 5MG

A cell-permeable sulfonamide. Blocks p53 interaction with Bcl-xL and Bcl-2 proteins and selectively inhibits p53 translocation to mitochondria without affecting the transactivation function of p53. Effectively protects against g radiation-induced cell death in vitro and animal lethality in vivo.

Quercetagetin. A cell-permeable flavanol compound that acts a potent, ATP-competitive, and reversible inhibitor of PIM1 kinase. Exhibits 7-fold selectivity over 8 other kinases tested, including PIM2. 5mg.

Leupeptin, Hemisulfate. (Ac-Leu-Leu-arginal, hemisulfate). A reversible inhibitor of trypsin-like proteases and cysteine proteases. Purity: =95% by HPLC. Effective concentration: 10-100uM. Soluble in water. CAS: 103476-89-7. FW: 475.6. White lyophilized solid, 100mg.

Leupeptin, Hemisulfate. (Ac-Leu-Leu-arginal, hemisulfate). A reversible inhibitor of trypsin-like proteases and cysteine proteases. Purity: =95% by HPLC. Effective concentration: 10-100uM. Soluble in water. CAS: 103476-89-7. FW: 475.6. White lyophilized solid, 10mg.

Leupeptin, Hemisulfate. (Ac-Leu-Leu-arginal, hemisulfate). A reversible inhibitor of trypsin-like proteases and cysteine proteases. Purity: =95% by HPLC. Effective concentration: 10-100uM. Soluble in water. CAS: 103476-89-7. FW: 475.6. White lyophilized solid, 25mg.

Leupeptin, Hemisulfate. (Ac-Leu-Leu-arginal, hemisulfate). A reversible inhibitor of trypsin-like proteases and cysteine proteases. Purity: =95% by HPLC. Effective concentration: 10-100uM. Soluble in water. CAS: 103476-89-7. FW: 475.6. White lyophilized solid, 50mg.

Leupeptin, Hemisulfate. (Ac-Leu-Leu-arginal, hemisulfate). A reversible inhibitor of trypsin-like proteases and cysteine proteases. Purity: =95% by HPLC. Effective concentration: 10-100uM. Soluble in water. CAS: 103476-89-7. FW: 475.6. White lyophilized solid, 5mg.

a1-Antichymotrypsin, Human Plasma. (a1-Achy; a1-1X; a1-1X-glycoprotein). Solid lyophilized from 150 mM NaCl, 20 mM Tris-HCl, pH 7.4. Acute-phase protein present at 45 mg/100 ml in plasma. Specific inhibitor of chymotrypsin-like serine proteinases. Activity: min.

a1-Antichymotrypsin, Human Plasma. (a1-Achy; a1-1X; a1-1X-glycoprotein). Solid lyophilized from 150 mM NaCl, 20 mM Tris-HCl, pH 7.4. Acute-phase protein present at 45 mg/100 ml in plasma. Specific inhibitor of chymotrypsin-like serine proteinases. Activity: min.

a1-Antitrypsin, Human Plasma. (a1-AT; a1-proteinase inhibitor; 3.5S a1-glycoprotein). Lyophilized from 300 mM NaCl, 30 mM sodium phosphate, pH 6.5.

a1-Antitrypsin, Human Plasma. (a1-AT; a1-proteinase inhibitor; 3.5S a1-glycoprotein). Lyophilized from 300 mM NaCl, 30 mM sodium phosphate, pH 6.5.

Cyclo(Arg-Gly-Asp-D-Phe-Val). (RGDFV Peptide, cyclic). White solid. Potent inhibitor of cell adhesion. Inhibits tumor cell adhesion to laminin and vitronectin substrates. In vivo investigations in rats showed it to be useful in the amelioration of ischemic acute renal failure in rats.

Calpastatin, Human, Recombinant. Lyophilized solid. Domain I of human calpastatin. Endogenous protease inhibitor that acts specifically on Calpain I (Cat. No. 208712). Exhibits greater inhibitory capacity than calpain inhibitors I and II. Purity: homogeneous by SDS-PAGE. Soluble in H2O. M.W.

Cathepsin L Inhibitor I. 1mg; White solid. A potent, cell-permeable, and irreversible inhibitor of Cathepsin L . Purity: 95% by TLC. Z-Phe-Phe-CH2F

E-64 Protease Inhibitor. Crystalline solid. Irreversible inhibitor of cysteine proteases. Has no action on cysteine residues in other proteins. Inhibits activation-induced programmed cell death and restores defective immune responses in HIV+ donors. Specific active site titrant.

E-64 Protease Inhibitor. Crystalline solid. Irreversible inhibitor of cysteine proteases. Has no action on cysteine residues in other proteins. Inhibits activation-induced programmed cell death and restores defective immune responses in HIV+ donors. Specific active site titrant.

E-64 Protease Inhibitor. Crystalline solid. Irreversible inhibitor of cysteine proteases. Has no action on cysteine residues in other proteins. Inhibits activation-induced programmed cell death and restores defective immune responses in HIV+ donors. Specific active site titrant.

Ecotin, E. coli. Liquid. In 1.0 mM HCl. A potent, broad range inhibitor of serine proteases. Exhibits picomolar binding constant for the inhibition of chymotrypsin, elastase, Factor Xa, Factor XIIa, kallikrein and trypsin. Also an effective inhibitor of collagenase and granzyme B.

Protease Inhibitor Cocktail Set I. HYGROSCOPIC. A cocktail of five protease inhibitors that will inhibit a broad range of proteases. Reconstitute each vial with 1 ml H2O to obtain a 100x stock solution. 1x stock solution contains. 500 -M AEBSF, HCl (Cat. No. 101500), 150 nM Aprotinin (Cat. No.

Protease Inhibitor Cocktail Set I. HYGROSCOPIC. A cocktail of five protease inhibitors that will inhibit a broad range of proteases. Reconstituted will yield 1mL of 100x stock soln; 1x solution contains 500uM AEBSF HCL, 150nM Aprotinin, 1uM E-64, 0.5mM EDTA disodium salt, and 1uM Leupeptin.

Protease Inhibitor Cocktail Set II. Lyophilized solid. HYGROSCOPIC. A cocktail of five protease inhibitors with broad specificity for the inhibition of aspartic, cysteine, serine, and metalloproteases as well as aminopeptidases. This cocktail is recommended for use with bacterial cell extracts.

Protease Inhibitor Cocktail Set II. Lyophilized solid. HYGROSCOPIC. A cocktail of five protease inhibitors with broad specificity for the inhibition of aspartic, cysteine, serine, and metalloproteases as well as aminopeptidases. This cocktail is recommended for use with bacterial cell extracts.

Protease Inhibitor Cocktail Set III. In 1 ml DMSO. A cocktail of six protease inhibitors with broad specificity for the inhibition of aspartic, cysteine, and serine proteases as well as aminopeptidases. This cocktail is recommended for use with mammalian cell and tissue extracts.

Protease Inhibitor Cocktail Set III. In 1 ml DMSO. A cocktail of six protease inhibitors with broad specificity for the inhibition of aspartic, cysteine, and serine proteases as well as aminopeptidases. This cocktail is recommended for use with mammalian cell and tissue extracts.

Paclitaxel, Taxus brevifolia. (Baccatin III N-benzyl-b-phenylisoserine ester). White solid. PROTECT FROM LIGHT. PROTECT FROM MOISTURE. Antitumor and antileukemic agent isolated from the bark of the yew tree. Promotes assembly of microtubules and inhibits tubulin disassembly.

Paclitaxel, Taxus brevifolia. (Baccatin III N-benzyl-b-phenylisoserine ester). White solid. PROTECT FROM LIGHT. PROTECT FROM MOISTURE. Antitumor and antileukemic agent isolated from the bark of the yew tree. Promotes assembly of microtubules and inhibits tubulin disassembly.

Paclitaxel, Taxus brevifolia. (Baccatin III N-benzyl-b-phenylisoserine ester). White solid. PROTECT FROM LIGHT. PROTECT FROM MOISTURE. Antitumor and antileukemic agent isolated from the bark of the yew tree. Promotes assembly of microtubules and inhibits tubulin disassembly.

Trypsin Inhibitor, Corn. In 30 mM NaCl, 20 mM Tris-HCl, pH 8.2. AVOID FREEZE/THAW CYCLES. Specific inhibitor of human Factor XIIa. Soluble in aqueous buffers. Molecular Weight: 14,000. WARNING! May cause irritation.

Trypsin Inhibitor, Soybean. Lyophilized solid. PROTECT FROM MOISTURE. Activity: 7000 units/mg dry weight. One unit is defined as the amount of protein that will inhibit 1.0 unit of trypsin activity using BAEE as a substrate at 25[degree] C, pH 7.6. Soluble in aqueous buffers. CAS 9035-81-8, M.W.

Trypsin Inhibitor, Soybean. Lyophilized solid. PROTECT FROM MOISTURE. Activity: 7000 units/mg dry weight. One unit is defined as the amount of protein that will inhibit 1.0 unit of trypsin activity using BAEE as a substrate at 25[degree] C, pH 7.6. Soluble in aqueous buffers. CAS 9035-81-8, M.W.

Trypsin Inhibitor, Soybean, High Activity. Salt-free lyophilized solid. PROTECT FROM MOISTURE. Component VI of Rackis. Activity: 14,000 units/mg dry weight. One unit is defined as the amount of protein that will inhibit 1.0 unit of trypsin activity using BAEE as a substrate at 25[degree] C, pH 7.6.

Trypsin Inhibitor, Soybean, High Activity. Salt-free lyophilized solid. PROTECT FROM MOISTURE. Component VI of Rackis. Activity: 14,000 units/mg dry weight. One unit is defined as the amount of protein that will inhibit 1.0 unit of trypsin activity using BAEE as a substrate at 25[degree] C, pH 7.6.

5-Fluoro-2'-deoxyuridine. 5-Fluoro-2''-deoxyuridine. (FdUrd; FUdR; 5-FdU). White solid. Experimental anticancer agent shown to have activity against a variety of malignant neoplasms, including mouse mammary tumors and colorectal carcinomas. Soluble in aqueous buffers and H2O.

5-Fluorouracil. (5-FU). Potent antitumor agent. Inhibits aminoisobutyrate-pyruvate aminotransferase. Induces apoptosis of human primary and metastatic colon adenocarcinoma in vitro. Purity: =98% by titration. Soluble in DMF, DMSO, methanol and hot water. CAS: 51-21-8. FW: 130.1. White solid, 1g.

Iodoacetic Acid, Sodium. Off-white solid. PROTECT FROM MOISTURE. PACKAGED UNDER INERT GAS. Inhibits cysteine proteases. Purity: = 98% by titration. Soluble in H2O. RTECS AI3675000, CAS 305-53-3, M.W. 207.9. WARNING! Toxic. LD50 of = 200 mg/kg. May be carcinogenic/teratogenic.

Phenylmethylsulfonyl Fluoride. (PMSF; benzylsulfonyl fluoride). Irreversible inhibitor of serine proteases. Its mechanism of action is analogous to that of diisopropylfluorophosphate. Purity: =98% by TLC. Soluble in ethanol, isopropanol, and methanol. CAS: 329-98-6. FW: 174.2. White solid, 1g.

Phenylmethylsulfonyl Fluoride. (PMSF; benzylsulfonyl fluoride). Irreversible inhibitor of serine proteases. Its mechanism of action is analogous to that of diisopropylfluorophosphate. Purity: =98% by TLC. Soluble in ethanol, isopropanol, and methanol. CAS: 329-98-6. FW: 174.2. White solid, 25g.

Phenylmethylsulfonyl Fluoride. (PMSF; benzylsulfonyl fluoride). Irreversible inhibitor of serine proteases. Its mechanism of action is analogous to that of diisopropylfluorophosphate. Purity: =98% by TLC. Soluble in ethanol, isopropanol, and methanol. CAS: 329-98-6. FW: 174.2. White solid, 5g.

ALLN. Inhibitor of calpain I (Ki=190nM), calpain II (Ki=220nM), cathepsin B (Ki=150nM) and cathepsin L (Ki=0.5nM). Purity: Single spot by TLC. Soluble in DMSO and ethanol. CAS: 110044-82-1. FW: 383.5. 25mg white solid.

ALLN. Inhibitor of calpain I (Ki=190nM), calpain II (Ki=220nM), cathepsin B (Ki=150nM) and cathepsin L (Ki=0.5nM). Purity: Single spot by TLC. Soluble in DMSO and ethanol. CAS: 110044-82-1. FW: 383.5. 5mg white solid.

Elastatinal. Yellow solid. Elastase-like serine protease inhibitor produced by actinomycetes. Inhibits PMSF-stimulated degradation of histone H1 and HMG proteins. Also inhibits a2 - macroglobulin-protease complexes.

Antipain, HCl. Pale yellow solid. Peptidyl arginine aldehyde protease inhibitor produced by actinomycetes. Inhibitor of Ca2+-dependent endopeptidases. Has specificity similar to Leupeptin (Cat. No. 108975). Inhibits trypsin-like serine proteases, papain and some cysteine proteases (IC50 = 300 mM).

Antipain, HCl. Pale yellow solid. Peptidyl arginine aldehyde protease inhibitor produced by actinomycetes. Inhibitor of Ca2+-dependent endopeptidases. Has specificity similar to Leupeptin (Cat. No. 108975). Inhibits trypsin-like serine proteases, papain and some cysteine proteases (IC50 = 300 mM).

Apigenin. (4'' ,5,7-Trihydroxyflavone). Crystalline solid. Induces the reversion of transformed phenotypes of v-H-ras-transformed NIH 3T3 cells at low concentration (12.5 mM). This finding has been attributed to the inhibition of MAP kinase activity.

p-APMSF, HCl. (p-Amidinophenylmethylsulfonylfluoride, HCl). White solid. Alternative to DFP and PMSF. Specific irreversible inhibitor of trypsin-like serine proteases. Inhibits trypsin and thrombin in equimolar concentration.

Bestatin. ( {[(2S,3R)-3-Amino-2-hydroxy-4-phenylbutanoyl]-Leu}). White solid. Binds to cell surfaces and inhibits surface aminopeptidases, notably aminopeptidase B and leucine aminopeptidase. Also acts as a potent aminopeptidase N inhibitor. Activates macrophages and T lymphocytes.

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