calcein am excitation emission

Calcein AM

1755-250
EUR 327

Calcein AM

1755-50
EUR 131

Calcein-AM

HY-D0041 100ug
EUR 147

Calcein-AM

GT0291-1MG 1 mg
EUR 341

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
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12352200

Calcein UltraGreen™ AM

21905 10x50 ug
EUR 219
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12352200

Calcein UltraBlue™ AM

21908 10x50 ug
EUR 219
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12352200

Calcein AM, 4mm in anhydrous DMSO

80011-1 100uL
EUR 226
Description: Minimum order quantity: 1 unit of 100uL

FALCON® CALCEIN AM FLUORESCENT DYE, 1MG

354217 1/pk
EUR 302
Description: Permeable Support - DL; Coated Transwells - DL

Calcein AM, 1mg/ml in anhydrous DMSO

80011-2 1ML
EUR 231
Description: Minimum order quantity: 1 unit of 1ML

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

EZViable? Calcein AM Cell Viability Assay Kit (Fluorometric)

K305-1000
EUR 359

Calcein

HY-D0040 100mg
EUR 119

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 Blue

HY-101887 25mg
EUR 119

Calcein (tetraethyl ester)

HY-D0830 25mg
EUR 257

Calcein Deep Red™

21902 1 mg
EUR 219
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12352200

Calcein Orange™ diacetate

22009 1 mg
EUR 219
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12352200

cAMP AM

20300 1 mg
EUR 50
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12352200

BAPTA AM

2242-25
EUR 262

BAPTA AM

2242-5
EUR 109

NAADP-AM

20997 2X50 ug
EUR 306
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12352200

NAADP-AM

20998 250 ug
EUR 393
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12352200

NAADP-AM

21000 1 mg
EUR 876
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12352200

BCECF, AM

21202 1 mg
EUR 176
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12352200

AM-679

B2521-1
EUR 153

AM-679

B2521-5
EUR 430

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-095

9581-25
EUR 588

AM-095

9581-5
EUR 185

AM resin

20-abx095149
  • EUR 314.00
  • EUR 592.00
  • EUR 885.00
  • 100 g
  • 250 g
  • 500 g
  • Shipped within 5-10 working days.

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).

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.

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-2394

HY-100221 10mM/1mL
EUR 216

BAPTA-AM

HY-100545 50mg
EUR 436

AM-4668

HY-12585 5mg
EUR 371

AM-1638

HY-13467 5mg
EUR 452

AM 103

HY-14163 1mg
EUR 2254

EGTA-AM

HY-D0973 5mg
EUR 587

AM-2099

HY-100727 10mM/1mL
EUR 361

BCECF-AM

HY-101883 1mg
EUR 316

AM-0902

HY-108329 100mg
EUR 1153

RT-AM

HY-108715A 1mg
EUR 452

SBFI-AM

GK8201-1MG 1 mg
EUR 628

AM-251

B2718-25 25 mg
EUR 510

AM-251

B2718-5 5 mg
EUR 166

Calcein Red™ sodium salt

21901 1 mg
EUR 219
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12352200

Calcein UltraBlue™ sodium salt

21909 1 mg
EUR 219
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12352200

Calcein Orange™ sodium salt

22008 1 mg
EUR 219
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12352200

Fluo-2, AM

20494 10x50 ug
EUR 176
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12352200

Fluo-2, AM

20495 1 mg
EUR 219
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12352200

FURA-2 Am

2243-1
EUR 262

FURA-2 Am

2243-set
EUR 153

Rhod-FF, AM

21077 1 mg
EUR 306
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12352200

Rhod-FF, AM

21078 10x50 ug
EUR 219
  • R-phrase: R20, R21, R22
  • H-Phrase: H303, H313, H333
  • Symbol for dangerous compounds: Xn
  • UNSPEC Code: 12352200

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

BCECF, AM ester

51012 1MG
EUR 137
Description: Minimum order quantity: 1 unit of 1MG

AM-92016 Hydrochloride

B2569-25
EUR 631

AM-92016 Hydrochloride

B2569-5
EUR 196

AM-095 Sodium

B1225-25
EUR 631

AM 92016 hydrochloride

B6482-10 10 mg
EUR 318
Description: AM 92016 hydrochloride is a specific inhibitor of delayed rectifier potassium current [1]. Potassium channel is an ion channel and acts to reset the resting potential and shapes the action potential.

FURA-4F/AM

9550-50
EUR 131

FURA-4F/AM

9550-set
EUR 349

FURA-5F/AM

9551-50
EUR 137