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Calcium Am Biotium

BAPTA, AM ester
50000-1 20MG
EUR 291.6
Description: Minimum order quantity: 1 unit of 20MG

Biotium Laboratories manufactures the calcium am biotium reagents distributed by Genprice. The Calcium Am Biotium reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact Biotium. Other Calcium products are available in stock. Specificity: Calcium Category: Am Group: Biotium

BCECF, AM ester 1mg/ml in dry DMSO
1ML
EUR 186
Description: Minimum order quantity: 1 unit of 1ML

Calcein AM Cell Viability Assay Kit (1000 assays)
1KIT
EUR 361.2
Description: Minimum order quantity: 1 unit of 1KIT

Calcium calibration buffer
1KIT
EUR 261.6
Description: Minimum order quantity: 1 unit of 1KIT

Ionomycin, calcium salt: (1mg)
1MG
EUR 244.8
Description: Minimum order quantity: 1 unit of 1MG

DMNP-EDTA(caged calcium)
5MG
EUR 284.4
Description: Minimum order quantity: 1 unit of 5MG

CD7 (T-Cell Leukemia Marker) (HuLy-m2) Antibody
500uL
EUR 652.8
Description: Primary antibody against CD7 (T-Cell Leukemia Marker)(HuLy-m2), CF594 conjugate, Concentration: 0.1mg/mL

Neurofilament phospho (NF-H) (Neuronal Marker) (NE14) Antibody
100uL
EUR 238.8
Description: Primary antibody against Neurofilament, phospho (NF-H) (Neuronal Marker) ( NE14), CF594 conjugate, Concentration: 0.1mg/mL

Biotium information

AM 114
A8163-5.1 10 mM (in 1mL DMSO)
EUR 129.6
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 338.4
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 97.2
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-251
B2718-25 25 mg
EUR 612

AM-251
B2718-5 5 mg
EUR 199.2

BAPTA-AM
B4758-10 10 mg
EUR 153.6
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 170.4
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 390
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 192

BCECF-AM
B5370-25 25 mg
EUR 2533.2

BCECF-AM
B5370-5 5 mg
EUR 654

AM 281
B6603-10 10 mg
EUR 234
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 150
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 762
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 502.8
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 313.2
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 282
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.