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Showing 312 to 500 of 20 results

Product	Utech#	UOM	Mfg#	Price
Oleoyl-L-Alpha-Lysophosphatidic Acid Sodium Salt, Each	10530292	EA	J66836LB0	$ 254.30
Ethylenediaminetetraacetic Acid (0.5M Solution/Ph 8.0), Fisher Bioreagents, Each	10530346	EA	BP24821	$ 382.28
Cas# 12030-85-2. 10G. Potassium Niobate (99.999%-Nb) Puratrem. Mfcd00049651, Each	10530357	EA	93411710G	$ 249.89
Cas# 7772-99-8. 500G. Tin(Ii) Chloride, Anhydrous, 98%. Mfcd00011241, Each	10530358	EA	935030500G	$ 244.42
Potassium Hydroxide, Certified, 0.1000N ±0.0005N (0.1M), Labchem, Each	10530362	EA	LC193006	$ 400.52
Calbiochem Apamin, Bee Venom, Polypeptide Neurotoxin Known To Pass Through The Blood-Brain Barrier, Each	10530418	EA	178270500UG	$ 270.93
Calbiochem™ Bisindolylmaleimide I, Each	10530420	EA	2032901MG	$ 275.03
Calbiochem Bisindolylmaleimide I, Hydrochloride, An Enhanced Water-Soluble Form Of Bisindolylmaleimide I, Each	10530421	EA	2032911MG	$ 275.03
Calbiochem™ Bmp Inhibitor Ii, Dmh1, Each	10530422	EA	2036465MG	$ 313.00
Calbiochem™ Ng,Ng-Dimethyl-L-Arginine, Dihydrochloride, Each	10530430	EA	31120325MG	$ 275.03
Calbiochem™ E2F Inhibitor, Hlm006474, Each	10530432	EA	32446110MG	$ 301.42
Calbiochem Camptothecin, 10-Hydroxy-, Camptotheca Acuminata, A Cell-Permeable Powerful Dna Topoisomerase I Inhibitor., Each	10530436	EA	39023825MG	$ 275.04
Calbiochem Kn-93, A Cell-Permeable, Reversible And Competitive Inhibitor Of Rat Brain Cam Kinase Ii (Ki = 370 Nm)., Each	10530439	EA	4227081MG	$ 275.03
Calbiochem Kn-92, Kn-92, Cas 1135280-28-2, Is Useful As A Negative Control For Kn-93 (Cat. No. 422708), A Ca2 /Cam Kinase Ii Inhibitor., Each	10530440	EA	4227091MG	$ 275.03
Calbiochem Pd 169316, A Potent, Cell-Permeable, Reversible, Competitive, And Selective P38 Map Kinase Inhibitor (Ic50 = 89 Nm)., Each	10530449	EA	5130301MG	$ 275.03
Calbiochem™ Insolution™ Pkr Inhibitor, Each	10530450	EA	5274515MG	$ 309.00
Calbiochem Ros Inhibitor, Ycg063, The Ros Inhibitor, Ycg063, Also Referenced Under Cas 330997-95-0, Controls The Biological Activity Of Ros, Each	10530454	EA	5573545MG	$ 302.48
Calbiochem Sod1 Inhibitor, Lcs-1, The Sod1 Inhibitor, Lcs-1, Also Referenced Under Cas 41931-13-9, Controls The Biological Activity Of Sod1, Each	10530459	EA	56741710MG	$ 309.00
Calbiochem™ Tgf-Β Ri Kinase Inhibitor Ii, Each	10530467	EA	6164522MG	$ 309.00
Calbiochem™ Trpml Agonist, Ml-Sa1, Each	10530468	EA	64849325MG	$ 290.76

Oleoyl-L-Alpha-Lysophosphatidic Acid Sodium Salt, Each

Ethylenediaminetetraacetic Acid (0.5M Solution/Ph 8.0), Fisher Bioreagents, Each

Cas# 12030-85-2. 10G. Potassium Niobate (99.999%-Nb) Puratrem. Mfcd00049651, Each

Cas# 7772-99-8. 500G. Tin(Ii) Chloride, Anhydrous, 98%. Mfcd00011241, Each

Potassium Hydroxide, Certified, 0.1000N ±0.0005N (0.1M), Labchem, Each

Calbiochem Apamin, Bee Venom, Polypeptide Neurotoxin Known To Pass Through The Blood-Brain Barrier, Each

Calbiochem™ Bisindolylmaleimide I, Each

Calbiochem Bisindolylmaleimide I, Hydrochloride, An Enhanced Water-Soluble Form Of Bisindolylmaleimide I, Each

Calbiochem™ Bmp Inhibitor Ii, Dmh1, Each

Calbiochem™ Ng,Ng-Dimethyl-L-Arginine, Dihydrochloride, Each

Calbiochem™ E2F Inhibitor, Hlm006474, Each

Calbiochem Camptothecin, 10-Hydroxy-, Camptotheca Acuminata, A Cell-Permeable Powerful Dna Topoisomerase I Inhibitor., Each

Calbiochem Kn-93, A Cell-Permeable, Reversible And Competitive Inhibitor Of Rat Brain Cam Kinase Ii (Ki = 370 Nm)., Each

Calbiochem Kn-92, Kn-92, Cas 1135280-28-2, Is Useful As A Negative Control For Kn-93 (Cat. No. 422708), A Ca2 /Cam Kinase Ii Inhibitor., Each

Calbiochem Pd 169316, A Potent, Cell-Permeable, Reversible, Competitive, And Selective P38 Map Kinase Inhibitor (Ic50 = 89 Nm)., Each

Calbiochem™ Insolution™ Pkr Inhibitor, Each

Calbiochem Ros Inhibitor, Ycg063, The Ros Inhibitor, Ycg063, Also Referenced Under Cas 330997-95-0, Controls The Biological Activity Of Ros, Each

Calbiochem Sod1 Inhibitor, Lcs-1, The Sod1 Inhibitor, Lcs-1, Also Referenced Under Cas 41931-13-9, Controls The Biological Activity Of Sod1, Each

Calbiochem™ Tgf-Β Ri Kinase Inhibitor Ii, Each

Calbiochem™ Trpml Agonist, Ml-Sa1, Each

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