calcein-am

177  

Calcein AM
1755-50
EUR 131

Calcein-AM
GT0291-1MG 1 mg
EUR 341

Calcein-AM
HY-D0041 100ug
EUR 147

Calcein AM (Calcein acetoxymethyl ester)
B7755-.5 500 µg
EUR 132

Calcein AM (Calcein acetoxymethyl ester)
B7755-1 1 mg
EUR 206

Calcein AM, (20x50ug)
80011-3 20ST
EUR 242
Description: Minimum order quantity: 1 unit of 20ST

Calcein Red™ AM
21900 1 mg
EUR 219

Calcein UltraGreen™ AM
21905 10x50 ug
EUR 219

Calcein UltraBlue™ AM
21908 10x50 ug
EUR 219

Calcein AM, 4mm in anhydrous DMSO
80011-1 100uL
EUR 226
Description: Minimum order quantity: 1 unit of 100uL

Calcein AM, 1mg/ml in anhydrous DMSO
80011-2 1ML
EUR 231
Description: Minimum order quantity: 1 unit of 1ML

FALCON® CALCEIN AM FLUORESCENT DYE, 1MG
354217 1/pk
EUR 302
Description: Permeable Support - DL; Coated Transwells - DL

EZViable? Calcein AM Cell Viability Assay Kit (Fluorometric)
K305-1000
EUR 359

Calcein AM Cell Viability Assay Kit (1000 assays)
30026 1KIT
EUR 301
Description: Minimum order quantity: 1 unit of 1KIT

FALCON® CALCEIN AM FLUORESCENT DYE, 500µG, 10X50µG
354216 1/pk
EUR 273
Description: Permeable Support - DL; Coated Transwells - DL

Calcein
GK2524-100G 100 g
EUR 329

Calcein
GK2524-10G 10 g
EUR 94

Calcein
GK2524-1G 1 g
EUR 50

Calcein
GK2524-25G 25 g
EUR 150

Calcein
GK2524-5G 5 g
EUR 70

Calcein
HY-D0040 100mg
EUR 119

Calcein Blue
HY-101887 25mg
EUR 119

Calcein (tetraethyl ester)
HY-D0830 25mg
EUR 257

Calcein Deep Red™
21902 1 mg
EUR 219

Calcein Orange™ diacetate
22009 1 mg
EUR 219

AM-095
9581-25
EUR 588

AM-095
9581-5
EUR 185

AM-251
B2718-25 25 mg
EUR 510

AM-251
B2718-5 5 mg
EUR 166

BAPTA AM
2242-25
EUR 262

BAPTA AM
2242-5
EUR 109

AM-679
B2521-1
EUR 153

AM-679
B2521-5
EUR 430

cAMP AM
20300 1 mg
EUR 50

NAADP-AM
20997 2X50 ug
EUR 306

NAADP-AM
20998 250 ug
EUR 393

NAADP-AM
21000 1 mg
EUR 876

BCECF, AM
21202 1 mg
EUR 176

AM resin
20-abx095149
  • EUR 314.00
  • EUR 592.00
  • EUR 885.00
  • 100 g
  • 250 g
  • 500 g

SBFI-AM
GK8201-1MG 1 mg
EUR 628

AM 103
HY-14163 1mg
EUR 2254

AM-0902
HY-108329 100mg
EUR 1153

RT-AM
HY-108715A 1mg
EUR 452

AM-4668
HY-12585 5mg
EUR 371

AM-1638
HY-13467 5mg
EUR 452

AM-2394
HY-100221 10mM/1mL
EUR 216

BAPTA-AM
HY-100545 50mg
EUR 436

AM-2099
HY-100727 10mM/1mL
EUR 361

BCECF-AM
HY-101883 1mg
EUR 316

EGTA-AM
HY-D0973 5mg
EUR 587

AM 114
A8163-10 10 mg
EUR 119
Description: AM 114, a derivative of boronic chalcone, is a potent small-molecule inhibitor of the proteasome that inhibits the chymotrypsin-like activity of the 20S proteasome, with a value of 50% inhibition concentration IC50 of approximately 1 ?M

AM 114
A8163-25 25 mg
EUR 189
Description: AM 114, a derivative of boronic chalcone, is a potent small-molecule inhibitor of the proteasome that inhibits the chymotrypsin-like activity of the 20S proteasome, with a value of 50% inhibition concentration IC50 of approximately 1 ?M

AM 114
A8163-5.1 10 mM (in 1mL DMSO)
EUR 108
Description: AM 114, a derivative of boronic chalcone, is a potent small-molecule inhibitor of the proteasome that inhibits the chymotrypsin-like activity of the 20S proteasome, with a value of 50% inhibition concentration IC50 of approximately 1 ?M

AM 114
A8163-50 50 mg
EUR 282
Description: AM 114, a derivative of boronic chalcone, is a potent small-molecule inhibitor of the proteasome that inhibits the chymotrypsin-like activity of the 20S proteasome, with a value of 50% inhibition concentration IC50 of approximately 1 ?M

AM 114
A8163-S Evaluation Sample
EUR 81
Description: AM 114, a derivative of boronic chalcone, is a potent small-molecule inhibitor of the proteasome that inhibits the chymotrypsin-like activity of the 20S proteasome, with a value of 50% inhibition concentration IC50 of approximately 1 ?M

AM 1172
B7392-10 10 mg
EUR 235
Description: AM 1172 is a potent and selective inhibitor of stable anandamide uptake with IC50 of 2.43102.5 ?M and fatty acid amide hydrolase (FAAH) with Ki of 3.18 ?M. FAAH, is an integral membrane hydrolase that hydrolyzes bioactive amides.

AM 1172
B7392-100 100 mg
EUR 1414
Description: AM 1172 is a potent and selective inhibitor of stable anandamide uptake with IC50 of 2.43102.5 ?M and fatty acid amide hydrolase (FAAH) with Ki of 3.18 ?M. FAAH, is an integral membrane hydrolase that hydrolyzes bioactive amides.

AM 1172
B7392-5 5 mg
EUR 147
Description: AM 1172 is a potent and selective inhibitor of stable anandamide uptake with IC50 of 2.43102.5 ?M and fatty acid amide hydrolase (FAAH) with Ki of 3.18 ?M. FAAH, is an integral membrane hydrolase that hydrolyzes bioactive amides.

AM 1172
B7392-50 50 mg
EUR 830
Description: AM 1172 is a potent and selective inhibitor of stable anandamide uptake with IC50 of 2.43102.5 ?M and fatty acid amide hydrolase (FAAH) with Ki of 3.18 ?M. FAAH, is an integral membrane hydrolase that hydrolyzes bioactive amides.

BAPTA-AM
B4758-10 10 mg
EUR 128
Description: BAPTA-AM is a selective calcium chelator [1]. Ca2+ is one of the most ubiquitous and versatile intracellular signaling molecules that control numerous cellular processes such as neurotransmitter release, contraction of all muscle cell types and fertilization [4].

BAPTA-AM
B4758-5.1 10 mM (in 1mL DMSO)
EUR 142
Description: BAPTA-AM is a selective calcium chelator [1]. Ca2+ is one of the most ubiquitous and versatile intracellular signaling molecules that control numerous cellular processes such as neurotransmitter release, contraction of all muscle cell types and fertilization [4].

BAPTA-AM
B4758-50 50 mg
EUR 325
Description: BAPTA-AM is a selective calcium chelator [1]. Ca2+ is one of the most ubiquitous and versatile intracellular signaling molecules that control numerous cellular processes such as neurotransmitter release, contraction of all muscle cell types and fertilization [4].

BCECF-AM
B5370-1 1 mg
EUR 160

BCECF-AM
B5370-25 25 mg
EUR 2111

BCECF-AM
B5370-5 5 mg
EUR 545

AM 281
B6603-10 10 mg
EUR 195
Description: AM 281 is a potent and selective antagonist/inverse agonist of CB1 cannabinoid receptor with Ki values of 12 and 4200 nM for CB1 and CB2 receptors, respectively [1].CB1 cannabinoid receptor is a G protein-coupled receptor and is mainly expressed in the brain.

AM 281
B6603-5 5 mg
EUR 125
Description: AM 281 is a potent and selective antagonist/inverse agonist of CB1 cannabinoid receptor with Ki values of 12 and 4200 nM for CB1 and CB2 receptors, respectively [1].CB1 cannabinoid receptor is a G protein-coupled receptor and is mainly expressed in the brain.

AM 281
B6603-50 50 mg
EUR 635
Description: AM 281 is a potent and selective antagonist/inverse agonist of CB1 cannabinoid receptor with Ki values of 12 and 4200 nM for CB1 and CB2 receptors, respectively [1].CB1 cannabinoid receptor is a G protein-coupled receptor and is mainly expressed in the brain.

AM 404
B6604-100 100 mg
EUR 419
Description: AM 404 is a selective inhibitor of anandamide transport [1]. Also, it is an agonist of CB1 cannabinoid receptor and potential vanilloid type 1 (TRPV1).

AM 404
B6604-50 50 mg
EUR 261
Description: AM 404 is a selective inhibitor of anandamide transport [1]. Also, it is an agonist of CB1 cannabinoid receptor and potential vanilloid type 1 (TRPV1).

Calcein Red™ sodium salt
21901 1 mg
EUR 219

Calcein UltraBlue™ sodium salt
21909 1 mg
EUR 219

Calcein Orange™ sodium salt
22008 1 mg
EUR 219

FURA-4F/AM
9550-50
EUR 131

FURA-4F/AM
9550-set
EUR 349

FURA-5F/AM
9551-50
EUR 137

FURA-5F/AM
9551-set
EUR 398

Poricoic acid AM
TBW00284 10mg
EUR 1295

FURA-2 Am
2243-1
EUR 262

FURA-2 Am
2243-set
EUR 153

AM-92016 Hydrochloride
B2569-25
EUR 631

AM-92016 Hydrochloride
B2569-5
EUR 196

AM-095 Sodium
B1225-25
EUR 631

Fluo-2, AM
20494 10x50 ug
EUR 176

Fluo-2, AM
20495 1 mg
EUR 219

Rhod-5N, AM
21070 1 mg
EUR 263

Rhod-FF, AM
21077 1 mg
EUR 306

Rhod-FF, AM
21078 10x50 ug
EUR 219

BAPTA, AM ester
50000 25MG
EUR 205
Description: Minimum order quantity: 1 unit of 25MG

BAPTA, AM ester
50000-1 20MG
EUR 243
Description: Minimum order quantity: 1 unit of 20MG