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| Product | Description | |
|---|---|---|
| Ifenprodil Hemitartrate. | Vasodilator (cerebral and peripheral). Group: Biochemicals. Alternative Names: α-(4-Hydroxyphenyl)- β-methyl-4-(phenylmethyl)-1-piperidineethanol (2R,3R)-2,3-Dihydroxybutanedioate. Grades: Highly Purified. CAS No. 23210-58-4. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
| Ifenprodil Hemitartrate (Erythro-4-(2-(4-Benzylpiperidin-1-yl)-1-hydroxypropyl)phenol Hemitartrate) | A partial non-competitive antagonist highly selective for GluN1/N2B subtype nMDA receptors (IC50 = 0.15uM, maximal inhibition 90%) over other subtypes (IC50 = 39, 29, 76uM for GluN1/N2A, GluN1/N2C and GluN1/N2D subtype receptors, respectively). Frequently used in studies of various brain functions and disorders involving neural transmissions mediated by GluN1/N2B subtype nMDA receptors. Group: Biochemicals. Grades: Highly Purified. CAS No. 23210-58-4. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Ifenprodil tartrate | Ifenprodil tartrate is a typical noncompetitive NMDA receptor antagonist. Ifenprodil tartrate exerts high affinity at NR1A/NR2B receptors ( IC 50 =0.34 μM) over 400-fold than at NR1A/NR2A receptors ( IC 50 =146 μM) [1]. Ifenprodil tartrate inhibits GIRK (Kir3) , reduces inward currents through the basal GIRK activity. Ifenprodil tartrate has the potential to be a cerebral vasodilator [2]. Uses: Scientific research. Group: Natural products. CAS No. 23210-58-4. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-12882A. |  |
| Ifenprodil Tartrate | Ifenprodil is an atypical noncompetitive antagonist at the NMDA receptor, it interacts with high affinity at a homogeneous population of NMDA receptors in neonatal rat forebrain with IC50 of 0.3 μM. Uses: Adrenergic alpha-antagonists. Synonyms: Ifenprodil (tartrate). Grades: >98%. CAS No. 23210-58-4. Molecular formula: 2(C21H27NO2).C4H6O6. Mole weight: 800.98. |  |
| Iferanserin | Iferanserin (S-MPEC) is a selective 5-HT receptor ( serotonin receptor ) antagonist with an affinity for 5-HT 2A receptor. Iferanserin has the potential for internal hemorrhoid disease treatment [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: S-MPEC. CAS No. 58754-46-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-118557. | |
| Ifetroban | Ifetroban (BMS-180291) is an orally active antagonist of thromboxane A2 ( TXA2 ) or prostaglandin H2 ( PGH2 ) receptor. Ifetroban shows antiplatelet activity, and inhibits tumor cell migration without affecting cell proliferation. Ifetroban can be used for myocardial ischemia, hypertension, stroke, thrombosis, cardiomyopathy research [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BMS-180291. CAS No. 143443-90-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-105218. | |
| Ifetroban | Ifetroban is a selective Prostaglandin receptor and Thromboxane A2 receptor antagonist under the development of Bristol-Myers Squibb. Phase II clinical trials for the treatment of Asthma, Hepatorenal syndrome, Portal hypertension and Systemic scleroderma is on-going. Uses: Asthma; hepatorenal syndrome; portal hypertension; systemic scleroderma. Synonyms: Ifetroban; BMS 180291-02; BMS-180291; BMS180291; CHEMBL283100; BMS-180291;SCHEMBL9589119;3-[2-[[3-[4-(pentylcarbamoyl)-1,3-oxazol-2-yl]-7-oxabicyclo[2.2.1]heptan-2-yl]methyl]phenyl]propanoic acid. Grades: 98%. CAS No. 143443-90-7. Molecular formula: C25H32N2O5. Mole weight: 440.54. | |
| Ifetroban sodium | Ifetroban (BMS-180291) sodium is an orally active antagonist of thromboxane A2 ( TXA2 ) or prostaglandin H2 ( PGH2 ) receptor. Ifetroban sodium shows antiplatelet activity, and inhibits tumor cell migration without affecting cell proliferation. Ifetroban sodium can be used for myocardial ischemia, hypertension, stroke, thrombosis, cardiomyopathy research [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BMS-180291 sodium. CAS No. 156715-37-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-105218A. | |
| Ifetroban sodium | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Ifinatamab | Ifinatamab is monoclonal immunoglobulin G1-kappa with anti-human B7 homolog 3 protein (Human B7-H3). Ifinatamab is a glycoforme α immunomodulateur [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2484870-90-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99367. | |
| Ifinatamab deruxtecan | Ifinatamab deruxtecan (DS-7300a) is an ADC that binds an anti-B7-H3 antibody to the DNA topoisomerase I inhibitory anti-tumor drug DXd. Ifinatamab deruxtecan has antitumor activity [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: DS-7300a; MABX-9001a. CAS No. 2484870-92-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P3371. | |
| Iflab-bb f2108-0112 | Iflab-bb f2108-0112. Uses: Designed for use in research and industrial production. Additional or Alternative Names: IFLAB-BB F2108-0112;2-CHLORO-1-PYRIDIN-4-YL-ETHANONE HCL. Product Category: Heterocyclic Organic Compound. CAS No. 25260-36-0. Molecular formula: C7H7Cl2NO. Product ID: ACM25260360. Alfa Chemistry ISO 9001:2015 Certified. |  |
| IFLAB-BB F2108-0142 | IFLAB-BB F2108-0142. Uses: Designed for use in research and industrial production. Additional or Alternative Names: IFLAB-BB F2108-0142;(2-FLUORO-PHENYL)-PROPYNOIC ACID. Product Category: Heterocyclic Organic Compound. CAS No. 704-97-2. Molecular formula: C9H5FO2. Product ID: ACM704972. Alfa Chemistry ISO 9001:2015 Certified. | |
| Iflab-bb f2124-0045 | Iflab-bb f2124-0045. Uses: Designed for use in research and industrial production. Additional or Alternative Names: IFLAB-BB F2124-0045;5-BROMO-2-METHOXY-PYRIMIDINE-4-CARBOXYLIC ACID. Product Category: Heterocyclic Organic Compound. CAS No. 38275-37-5. Molecular formula: C6H5BrN2O3. Mole weight: 233.02. Product ID: ACM38275375. Alfa Chemistry ISO 9001:2015 Certified. Categories: 5-bromo-2-methoxypyrimidine-4-carboxylic acid. | |
| Iflab-bb f2124-0085 | Iflab-bb f2124-0085. Uses: Designed for use in research and industrial production. Additional or Alternative Names: IFLAB-BB F2124-0085;6-CHLORO-N4-CYCLOHEXYL-PYRIMIDINE-4,5-DIAMINE;(5-amino-6-chloro-pyrimidin-4-yl)-cyclohexyl-amine;6-chloro-4-N-cyclohexylpyrimidine-4,5-diamine. Product Category: Heterocyclic Organic Compound. CAS No. 5449-10-5. Molecular formula: C10H15ClN4. Mole weight: 226.71. Product ID: ACM5449105. Alfa Chemistry ISO 9001:2015 Certified. | |
| IFN-alpha 1 human | recombinant, expressed in E. coli, ?95% (SDS-PAGE), ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| IFN-alpha 2a human | recombinant, expressed in E. coli, ?95% (SDS-PAGE), ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| IFN-alpha 2b human | recombinant, expressed in E. coli, ?98% (SDS-PAGE), ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| IFN alpha-IFNAR-IN-1 | IFN alpha-IFNAR-IN-1 is a nonpeptidic, low-molecular-weight inhibitor. It inhibits MVA-induced IFN-α responses by BM-pDCs (IC50=2-8 uM). It exerts immunosuppressive activity by the direct interaction with IFN-&alpha. Uses: Ifn alpha-ifnar-in-1 inhibits mva-induced ifn-α responses by bm-pdcs. it exerts immunosuppressive activity by the direct interaction with ifn-&alpha. Synonyms: IFN-alpha; IFN alpha; IFNAR-IN-1; IFNAR IN 1; IFNARIN1; IFNAR inhibitor 1; IFNAR-inhibitor-1; IFN-alpha and IFNAR interaction inhibitor. Grades: >98%. CAS No. 844882-93-5. Molecular formula: C18H17NS. Mole weight: 279.40. | |
| IFN alpha-IFNAR-IN-1 hydrochloride | IFN alpha-IFNAR-IN-1 hydrochloride is a nonpeptidic, low-molecular-weight inhibitor of the interaction between IFN-? and IFNAR. IFN alpha-IFNAR-IN-1 hydrochloride inhibits modified Vaccinia virus ankara (MVA)-induced IFN-? responses in murine bone-marrow-derived, Flt3- L-differentiated pDC cultures (BM-pDCs) (IC50=2-8 ?M)[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2070014-98-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-12836A. | |
| IFN alpha-IFNAR-IN-1 hydrochloride | IFN alpha-IFNAR-IN-1 hydrochloride is a nonpeptidic, low-molecular-weight inhibitor. It inhibits modified Vaccinia virus ankara (MVA)-induced IFN-α responses in murine bone-marrow-derived, Flt3-L-differentiated pDC cultures (BM-pDCs) (IC50=2-8 μM). Synonyms: IFN-alpha/IFNAR-IN-1 hydrochloride. CAS No. 2070014-98-9. Molecular formula: C18H18ClNS. Mole weight: 315.86. | |
| IFN-γ Antagonist | IFN-γ Antagonist, derived from the ligand binding site of human γ-interferon (IFN-γ) receptor, is an antagonist of human IFN-γ, and inhibits human IFN-γ-induced expression of HLR/DR antigen on Colo 205 cells with an IC50 of about 35 μM. Synonyms: (Tyr121,Cys(Acm)122)-IFN-γ Receptor (120-141) (human); L-Isoleucine, L-alanyl-L-tyrosyl-S-[(acetylamino)methyl]-L-cysteinyl-L-arginyl-L-α-aspartylglycyl-L-lysyl-L-isoleucylglycyl-L-prolyl-L-prolyl-L-lysyl-L-leucyl-L-α-aspartyl-L-isoleucyl-L-arginyl-L-lysyl-L-α-glutamyl-L-α-glutamyl-L-lysyl-L-glutaminyl-; L-alanyl-L-tyrosyl-S-acetamidomethyl-L-cysteinyl-L-arginyl-L-alpha-aspartyl-glycyl-L-lysyl-L-isoleucyl-glycyl-L-prolyl-L-prolyl-L-lysyl-L-leucyl-L-alpha-aspartyl-L-isoleucyl-L-arginyl-L-lysyl-L-alpha-glutamyl-L-alpha-glutamyl-L-lysyl-L-glutaminyl-L-isoleucine; H-Ala-Tyr-Cys(Acm)-Arg-Asp-Gly-Lys-Ile-Gly-Pro-Pro-Lys-Leu-Asp-Ile-Arg-Lys-Glu-Glu-Lys-Gln-Ile-OH. Grades: ≥95%. CAS No. 158040-83-6. Molecular formula: C115H194N34O34S. Mole weight: 2629.04. | |
| IFN-γ Antagonist 1 | IFN-γ Antagonist 1 (AYCRDGKIGPPKLDIRKEEKQI) is an antagonist of interferon γ ( IFN γ ). IFN-γ Antagonist 1 inhibits IFN-γ induced HLR/DR antigen expression in Colon 205 cells with an IC 50 value of approximately 35 μM. IFN-γ Antagonist 1 has potential applications in immune regulation [1]. Uses: Scientific research. Group: Peptides. CAS No. 158040-83-6. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P4717. | |
| IFN-? human | Animal-component free, recombinant, expressed in E. coli, ?98% (SDS-PAGE), ?98% (HPLC), suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| IFN-LAMBDA1 human | Animal-component free, recombinant, expressed in E. coli, ?98% (SDS-PAGE), ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| IFN-lambda 2 from mouse | recombinant, expressed in E. coli, ?98% (SDS-PAGE), ?98% (HPLC), suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| IFN-lambda 2 human | recombinant, expressed in E. coli, ?98% (SDS-PAGE), ?98% (HPLC), suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| IFN-omega human | recombinant, expressed in E. coli, ?98% (SDS-PAGE), ?98% (HPLC), suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| Ifosfamide | Ifosfamide is an alkylating chemotherapeutic agent with activity against a wide range of tumors. Uses: Scientific research. Group: Signaling pathways. CAS No. 3778-73-2. Pack Sizes: 200 mg; 500 mg. Product ID: HY-17419. | |
| Ifosfamide | Ifosfamide is a nitrogen mustard alkylating agent used in the treatment of cancer. Uses: Antineoplastic agents, alkylating. Synonyms: 2H-1,3,2-Oxazaphosphorin-2-amine, N,3-bis(2-chloroethyl)tetrahydro-, 2-oxide; 2H-1,3,2-Oxazaphosphorine, 3-(2-chloroethyl)-2-[(2-chloroethyl)amino]tetrahydro-, 2-oxide; (2-Chloro-ethyl)-[3-(2-chloro-ethyl)-2-oxo-2λ*5*-[1,3,2]oxazaphosphinan-2-yl]-amine; (±)-Ifosfamide; 3-(2-Chloroethyl)-2-(2-chloroethylamino)tetrahydro-2H-1,3,2-oxazaphosphorine 2-oxide; A 4942; Asta Z 4942; Cyfos; Holoxan; Holoxan 1000; Ifex; Ifomide; Ifosfamid; Ifosfomide; Ifosphamide; Iphosphamide; Isoendoxan; Isofosfamide; Isophosphamide; Mitoxana; MJF 9325; Naxamide; NSC 109724; Z 4942. Grades: >98%. CAS No. 3778-73-2. Molecular formula: C7H15Cl2N2O2P. Mole weight: 261.09. | |
| Ifosfamide | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardspharma & vet compounds & metabolitespharma & vet compounds & metabolitesapi standardsbritish pharmacopoeiaeuropean pharmacopoeia (ph. eur.)pharmaceutical toxicologypharmacopoeial standards. Alternative Names: (RS)-N,3-bis(2-chloroethyl)-1,3,2-oxazaphosphinan-2-amine 2-oxide,Ifosfamide. | |
| Ifosfamide | 1g Pack Size. Group: Bioactive Small Molecules, Research Organics & Inorganics. Formula: C7H15Cl2N2O2P. CAS No. 3778-73-2. Prepack ID 43331190-1g. Molecular Weight 261.09. See USA prepack pricing. |  |
| Ifosfamide (Asta Z-4942, NSC-1097) | A cytostatic agent, related structurally to cyclophosphamide. Group: Biochemicals. Alternative Names: N,3-Bis(2-chloroethyl)tetrahydro-2H-1,3,2-oxazaphosphorin-2-amine 2-Oxide;A 4942; Asta Z 4942; Cyfos; Holoxan; Ifex; Ifomide; Iphosphamide; MJF 9325; Mitoxana; NSC 109724; Naxamide. Grades: Highly Purified. CAS No. 3778-73-2. Pack Sizes: 100mg, 250mg, 500mg, 1g. Molecular Formula: C7H15Cl2N2O2P, Molecular Weight: 261.09. US Biological Life Sciences. | Worldwide |
| Ifosfamide-d4 | A cytostatic agent, related structurally to cyclophosphamide. Group: Biochemicals. Alternative Names: N,3-Bis(2-chloroethyl)tetrahydro-2H-1,3,2-oxazaphosphorin-2-amine 2-Oxide-d4. Grades: Highly Purified. CAS No. 1189701-13-0. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Ifosfamide Impurity 1 | Grades: > 95%. Molecular formula: C8H17Cl2N2O2P. Mole weight: 275.12. | |
| Ifosfamide Impurity A | Synonyms: 3-[(2-chloroethyl)amino]propyl dihydrogen phosphate. Grades: > 95%. CAS No. 22608-58-8. Molecular formula: C5H13ClNO4P. Mole weight: 217.59. | |
| Ifosfamide Impurity B | Synonyms: Bis[3-[(2-chloroethyl)amino]propyl] dihydrogen diphosphate. Grades: > 95%. CAS No. 241482-18-8. Molecular formula: C10H24Cl2N2O7P2. Mole weight: 417.17. | |
| Ifosfamide Impurity E | Synonyms: 3-chloro-N-(2-chloroethyl)propan-1-amine. Grades: > 95%. CAS No. 42453-19-0. Molecular formula: C5H11Cl2N. Mole weight: 156.06. | |
| Ifosfamide Impurity F | Synonyms: Ifosfamide Impurity F; 81485-04-3. Grades: > 95%. CAS No. 81485-04-3. Molecular formula: C5H10Cl2NO2P. Mole weight: 218.02. | |
| Ifosfamide USP | Ifosfamide USP. Grades: USP. CAS No. 3778-73-2. Product ID: 8-04235. Molecular formula: C7H15Cl2N2O2P. Mole weight: 261.09. |  |
| iFSP1 | iFSP1 is a potent, selective and glutathione-independent inhibitor of ferroptosis suppressor protein 1 (FSP1) (AIFM2) with an EC50 of 103 nM. iFSP1 selectively induces ferroptosis in GPX4-knockout cells which overexpressed FSP1. iFSP1 is able to sensitize a variety of human cancer cell lines to the ferroptosis inducer, such as (1S,3R)-RSL3 (HY-100218A)[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 150651-39-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-136057. | |
| I+G | I+G. Group: Food ingredients. Pack Sizes: 10Kg Cartons. Categories: Inosinate and Guanylate). |  |
| IG-105 | IG-105 is a potent microtubule inhibitor with potential anticancer activity. IG-105 inhibits microtubule assembly by binding at colchicine pocket. IG-105 shows a potent anticancer activity in vitro and in vivo and has good safety in mice. IG-105 showed a potent activity against human leukemia and solid tumors in breast, liver, prostate, lung, skin, colon, and pancreas with IC(50) values between 0.012 and 0.298 mumol/L. It was also active in drug-resistant tumor cells and not a P-glycoprotein substrate. It inhibited microtubule assembly followed by M-phase arrest, Bcl-2 inactivation, and then apoptosis through caspase pathways. Synonyms: IG105; IG 105. Grades: 98%. CAS No. 905978-63-4. Molecular formula: C20H19N3O4S. Mole weight: 397.45. | |
| IgA from human serum | reagent grade, ?95% (HPLC), buffered aqueous solution. Group: Fluorescence/luminescence spectroscopy. | |
| IgA, Kappa from murine myeloma | clone TEPC 15, purified immunoglobulin, buffered aqueous solution. Group: Fluorescence/luminescence spectroscopy. | |
| IgA-specific metalloendopeptidase | A 190 kDa enzyme found in several pathogenic species of Streptococcus such as sanguis and pneumoniae. Type example of peptidase family M26. There is also an IgA-specific prolyl endopeptidase of the serine-type (see EC 3.4.21.72, IgA-specific serine endopeptidase). Group: Enzymes. Synonyms: immunoglobulin A1 proteinase; IgA protease; IgA1-specific proteinase; IgA1 protease; IgA1 proteinase. Enzyme Commission Number: EC 3.4.24.13. CAS No. 72231-73-3. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4294; IgA-specific metalloendopeptidase; EC 3.4.24.13; 72231-73-3; immunoglobulin A1 proteinase; IgA protease; IgA1-specific proteinase; IgA1 protease; IgA1 proteinase. Cat No: EXWM-4294. |  |
| IgA-specific serine endopeptidase | Species variants differing slightly in specificity are secreted by Gram-negative bacteria Neisseria gonorrhoeae and Haemophilus influenzae. Type example of peptidase family S6. Some other bacterial endopeptidases with similar specificity are of metallo- type (see EC 3.4.24.13, IgA-specific metalloendopeptidase). Group: Enzymes. Synonyms: IgA protease; IgA proteinase; IgA-specific proteinase; immunoglobulin A protease; immunoglobulin A proteinase. Enzyme Commission Number: EC 3.4.21.72. CAS No. 55127-02-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4164; IgA-specific serine endopeptidase; EC 3.4.21.72; 55127-02-1; IgA protease; IgA proteinase; IgA-specific proteinase; immunoglobulin A protease; immunoglobulin A proteinase. Cat No: EXWM-4164. | |
| IgdE protease | IgdE protease is a cysteine protease, which is initially isolated from Streptococcus agalactiae. IgdE protease digests monoclonal antibodies (mAbs) of the IgG1 type specifically at their upper hinge region, produces Fc/2, hinge peptide dimers, and Fab fragment. IgdE protease can be used in disulfide bonds and free thiol analysis, as it requires no reducing agents for cleavage [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1892548-76-3. Pack Sizes: 1 KU. Product ID: HY-E70364. | |
| Igepal CO-520 | Igepal CO-520. Group: Biochemicals. Alternative Names: Poly(oxy-1,2-ethanediyl),a-(nonylphenyl)-w-hydroxy-, Branched Polymer; α-(Nonylphenyl)-ω-hydroxy-poly(oxy-1,2-ethanediyl) Branched Polymer. Grades: Highly Purified. CAS No. 68412-54-4. Pack Sizes: 1g, 250g, 500g. US Biological Life Sciences. | Worldwide |
| IGF-1 DES1,3 | IGF-1 DES1,3 is a fragment of amino acids of the Insulin Growth Factor-1 DES. Synonyms: Insulin Growth Factor-1 DES. Grades: 99%. CAS No. 67763-96-6. Molecular formula: C18H32N5O7S1. Mole weight: 462.55. | |
| IGF-1 LR3 | IGF-1 LR3 is a lengthened analogue of human insulin-like growth factor 1 (IGF-1). Synonyms: Long R3-IGF-1; IGF-1 Long R3; Long arginine 3-IGF-1. Grades: 95%. CAS No. 946870-92-4. Molecular formula: C400H625N111O115S9. Mole weight: 9117.6. | |
| IGF1R (960-end), active, His tagged human | recombinant, expressed in baculovirus infected Sf9 cells, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. | |
| IGF-1R Inhibitor II, PQ401 - CAS 196868-63-0 | The IGF-1R Inhibitor II, also referenced under CAS 196868-63-0, controls the biological activity of IGF-1R. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications. Group: Fluorescence/luminescence spectroscopy. | |
| IGF-1R Inhibitor, PPP - CAS 477-47-4 | The IGF-1R Inhibitor, PPP, also referenced under CAS 477-47-4, controls the biological activity of IGF-1R. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications. Group: Fluorescence/luminescence spectroscopy. | |
| IGF-Binding Protein 1 human | recombinant, expressed in E. coli, ?98% (SDS-PAGE), ?98% (HPLC), suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| IGF-Binding Protein 2 human | recombinant, expressed in (BTI-Tn-5B1-4) High-5 Insect Cells, ?98% (SDS-PAGE), ?98% (HPLC), suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| IGF-Binding Protein-3 human | recombinant, expressed in E. coli, ?98% (SDS-PAGE), ?98% (HPLC), suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| IGF-Binding Protein 4 human | recombinant, expressed in (BTI-Tn-5B1-4) High-5 Insect Cells, ?98% (SDS-PAGE), ?98% (HPLC), suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| IGF-Binding Protein-5 human | recombinant, expressed in E. coli, ?98% (SDS-PAGE), ?98% (HPLC), suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| IGF-Binding Protein 6 human | recombinant, expressed in (BTI-Tn-5B1-4) High-5 Insect Cells, ?95% (SDS-PAGE), ?95% (HPLC), suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| IGF-Binding Protein 7 human | recombinant, expressed in E. coli, ?98% (SDS-PAGE), ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| IGF-I 24-41 | IGF-I 24-41 is a 24-41 amino acid fragment of insulin-like growth factor I(IGF-I). IGF-I has anabolic, antioxidant, anti-inflammatory and cell-protective properties. Synonyms: Insulin-like Growth Factor I (24-41); H-Tyr-Phe-Asn-Lys-Pro-Thr-Gly-Tyr-Gly-Ser-Ser-Ser-Arg-Arg-Ala-Pro-Gln-Thr-OH; L-tyrosyl-L-phenylalanyl-L-asparagyl-L-lysyl-L-prolyl-L-threonyl-glycyl-L-tyrosyl-glycyl-L-seryl-L-seryl-L-seryl-L-arginyl-L-arginyl-L-alanyl-L-prolyl-L-glutaminyl-L-threonine. Grades: ≥95%. CAS No. 135861-49-3. Molecular formula: C88H133N27O28. Mole weight: 2017.16. | |
| IGF-I 30-41 | IGF-I 30-41 is a 30-41 amino acid fragment of insulin-like growth factor I(IGF-I). IGF-I has anabolic, antioxidant, anti-inflammatory and cell-protective properties. Synonyms: Insulin-like Growth Factor I (30-41); H-Gly-Tyr-Gly-Ser-Ser-Ser-Arg-Arg-Ala-Pro-Gln-Thr-OH; glycyl-L-tyrosyl-glycyl-L-seryl-L-seryl-L-seryl-L-arginyl-L-arginyl-L-alanyl-L-prolyl-L-glutaminyl-L-threonine. Grades: ≥95%. CAS No. 82177-09-1. Molecular formula: C51H83N19O19. Mole weight: 1266.32. | |
| IGF-I 30-41 acetate | IGF-I 30-41 acetate is a 30-41 amino acid fragment of insulin-like growth factor I(IGF-I). IGF-I has anabolic, antioxidant, anti-inflammatory and cell-protective properties. Synonyms: Insulin-like Growth Factor I (30-41) acetate; H-Gly-Tyr-Gly-Ser-Ser-Ser-Arg-Arg-Ala-Pro-Gln-Thr-OH.CH3CO2H; glycyl-L-tyrosyl-glycyl-L-seryl-L-seryl-L-seryl-L-arginyl-L-arginyl-L-alanyl-L-prolyl-L-glutaminyl-L-threonine acetic acid. Grades: ≥95%. Molecular formula: C53H87N19O21. Mole weight: 1326.39. | |
| IGF-I from rat | recombinant, expressed in E. coli, ?95% (SDS-PAGE), ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| IGF-I human | Animal-component free, recombinant, expressed in E. coli, ?98% (SDS-PAGE), ?98% (HPLC), suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| IgG1, Kappa from human myeloma plasma | purified immunoglobulin, >95% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| IgG1, Lambda from human myeloma plasma | purified immunoglobulin, >95% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. | |
| IgG2a, Lambda from murine myeloma | clone HOPC-1, purified immunoglobulin, buffered aqueous solution. Group: Fluorescence/luminescence spectroscopy. | |
| IgG2b, Kappa from murine myeloma | clone MOPC 195, ascites fluid, lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
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