产品编号：4075430

纯度规格：AldrichCPR

包装规格：1 G

产品编号：4075428

纯度规格：AldrichCPR

包装规格：1 G

产品编号：4075401

纯度规格：For use as a marker in SDS-PAGE

包装规格：1 VIAL

产品编号：4075388

纯度规格：Swinnex Filter Holder, 47mm

包装规格：8 pkg

产品编号：4075385

包装规格：1 EA

产品编号：4075361

纯度规格：suitable for microbiology

包装规格：1 VIAL

产品编号：4075357

纯度规格：AldrichCPR

包装规格：1 G

产品编号：4075356

纯度规格：AldrichCPR

包装规格：1 G

产品编号：4075346

纯度规格：from human cervix, 11033105

包装规格：1 VIAL

产品编号：4075340

纯度规格：Aldrich^CPR

包装规格：1 G

产品编号：4075327

纯度规格：n = 1

包装规格：2.5 G

产品编号：4075326

纯度规格：n = 1

包装规格：1 G

产品编号：4075313

包装规格：1 EA

产品编号：4075311

包装规格：1 EA

产品编号：4075310

包装规格：1 EA

产品编号：4075309

包装规格：1 EA

产品编号：4075286

纯度规格：AldrichCPR

包装规格：1 G

产品编号：4075284

纯度规格：AldrichCPR

包装规格：1 G

产品编号：4075282

纯度规格：AldrichCPR

包装规格：1 G

产品编号：4075276

纯度规格：AldrichCPR

包装规格：1 G

产品编号：4075275

纯度规格：AldrichCPR

包装规格：1 G

产品编号：4075274

纯度规格：AldrichCPR

包装规格：1 G

产品编号：4075273

纯度规格：AldrichCPR

包装规格：1 G

产品编号：4075269

纯度规格：≥70% (SDS-PAGE), recombinant, expressed in baculovirus infected insect cells, buffered aqueous glycerol solution

包装规格：10 μG

产品编号：4075268

纯度规格：≥85%, lyophilized powder

包装规格：1 MG，5 X 1 MG

产品编号：4075267

纯度规格：A non-essential, optically inactive, non-chiral amino acid. Acts as an inhibitory neurotransmitter, particularly in brain stem and medulla.

包装规格：500 G，1 KG

产品编号：4075264

纯度规格：Substrate for fluorogenic assay of plasma and glandular kallikreins.

包装规格：25MG

产品编号：4075263

包装规格：1 MG

产品编号：4075262

纯度规格：A protective agent for SH groups.

包装规格：5 G

产品编号：4075261

纯度规格：DSPC, GMP, powder

包装规格：1 G

产品编号：4075260

纯度规格：Glutathione, Oxidized, Free Acid, CAS 27025-41-8, forms a "redox buffer" in physiological systems in the presence of reduced glutathione.

包装规格：1 G，5 G

产品编号：4075259

纯度规格：recombinant, expressed in Nicotiana, heat and acid-stable competitive, reversible inhibitor of serine proteases

包装规格：1 MG，5 MG，25 MG

产品编号：4075258

纯度规格：The JNK Inhibitor III, Cell-Permeable controls the biological activity of JNK. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.

包装规格：1 MG

产品编号：4075257

纯度规格：≥95% (HPLC)

包装规格：0.1 MG

产品编号：4075256

纯度规格：This γ-secretase inhibitor, CAS 209984-56-5, is a cell-permeable dibenzazepine compound that lowers both brain and plasma Aβ40 levels by ~72% in Tg2576 mutant APP transgenic mouse model.

包装规格：500 μG，1 MG

产品编号：4075255

纯度规格：Membrane-permeable version of FLUO 3. Unlike all other Ca²⁺ indicators, FLUO 3/AM is non-fluorescent until it is hydrolyzed in the cell by cellular esterases. It is insensitive to Mg²⁺.

产品编号：4075254

纯度规格：The Eg5 Inhibitor III, Dimethylenastron, also referenced under CAS 863774-58-7, controls the biological activity of Eg5. This small molecule/inhibitor is primarily used for Membrane applications.

包装规格：5 MG

产品编号：4075252

纯度规格：The Cdk1/2 Inhibitor II, NU6102, also referenced under CAS 444722-95-6, controls the biological activity of Cdk1/2. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.

包装规格：1 MG

产品编号：4075251

纯度规格：An enhanced water-soluble form of Bisindolylmaleimide I.

包装规格：1 MG

产品编号：4075250

纯度规格：The Akt Inhibitor IV, also referenced under CAS 681281-88-9, controls the biological activity of Akt. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.

包装规格：1 MG，5 MG

产品编号：4075249

纯度规格：SB 203580, Hydrochloride, CAS 869185-85-3, is a water-soluble form of SB 203580. A highly potent, selective, ATP-competitive inhibitor of p38 MAP Kinase (IC₅₀ = 34 nM in vitro, 600 nM in cells).

包装规格：1 MG，10 MG

产品编号：4075248

纯度规格：Inducer of β-D-galactosidase. Used in the stimulation of β-galactosidase in cellular systems in which dioxane would disrupt normal cell function. Contains no animal-derived products.

包装规格：1 G，5 G

产品编号：4075247

纯度规格：A potent mediator of inflammation that increases vascular permeability. Activates MAP kinases and MAP kinase kinase (MEK) in CHO cells.

包装规格：1 MG，5 MG

产品编号：4075246

纯度规格：An organomercurial agent used for the activation of latent MMPs in vitro. Acts by facilitating the loss of the enzyme propeptide domain through an autolytic cleavage known as the cysteine switch.

包装规格：700 MG

产品编号：4075245

纯度规格：InSolution Q-VD-OPh, Non-O-methylated, is a cell-permeable, irreversible, broad-spectrum inhibitor of caspases (IC₅₀ = 50, 100, 430, and <25 nM for caspase-1,-8, -9, and -3, respectively).

包装规格：1 MG，5 MG

产品编号：4075244

纯度规格：Gö 6976, CAS 136194-77-9, is a cell-permeable, reversible, and ATP-competitive inhibitor of PKC (IC₅₀ = 7.9 nM for rat brain). Exhibits selectively for PKCα (IC₅₀ = 2.3 nM) and βI (IC₅₀

包装规格：500 μG，1 MG

产品编号：4075243

包装规格：5 MG

产品编号：4075242

纯度规格：The DNA-PK Inhibitor V, also referenced under CAS 404009-46-7, controls the biological activity of DNA-PK. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.

包装规格：5 MG

产品编号：4075240

纯度规格：The Caspase-3 Inhibitor II, also referenced under CAS 210344-95-9, controls the biological activity of Caspase-3. This small molecule/inhibitor is primarily used for Cancer applications.

包装规格：250 μG，1 MG

产品编号：4075239

纯度规格：The Caspase Inhibitor III, also referenced under CAS 634911-80-1, controls the biological activity of Caspase. This small molecule/inhibitor is primarily used for Cancer applications.

包装规格：250 μG，1 MG