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acids+and+salts+high+purity
Numéro de catalogue:
(AATB20515)
Fournisseur:
AAT BIOQUEST INC
Description:
Calcium measurement is critical for numerous biological investigations.
UOM:
1 * 250 µG
New Product
Fournisseur:
AAT BIOQUEST INC
Description:
Calcium measurement is critical for numerous biological investigations.
Fournisseur:
MP Biomedicals
Description:
5-Phosphorylribose-1-pyrophosphate Sodium Salt Hydrate has been used in a study to assess the relationship between the muscarinic receptor cationic current and internal calcium in guinea-pig jejunal smooth muscle cells. It has also been used in a study to investigate inhibitors of the bacterial cell wall biosynthesis of the enzyme Mur D.
Numéro de catalogue:
(AATB295)
Fournisseur:
AAT BIOQUEST INC
Description:
This Cy7® dye is the same molecule to GE's Cy7® bisNHS ester.
UOM:
1 * 1 mg
New Product
Numéro de catalogue:
(AATB21144)
Fournisseur:
AAT BIOQUEST INC
Description:
Cal-520® provides a robust homogeneous fluorescence-based assay tool for detecting intracellular calcium mobilization.
UOM:
1 * 500 µG
New Product
Numéro de catalogue:
(AATB20380)
Fournisseur:
AAT BIOQUEST INC
Description:
Mag-Fura-2, tetrapotassium salt is an intracellular magnesium indicator that is ratiometric and UV light-excitable.
UOM:
1 * 1 mg
New Product
Numéro de catalogue:
(BOSSBS-13627R-FITC)
Fournisseur:
Bioss
Description:
The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter’s syndrome which is characterized by renal salt-wasting and low blood pressure.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-10307R-CY3)
Fournisseur:
Bioss
Description:
The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport and maintain cellular volume. The genes encoding human CLC-1 through CLC-7 map to chromosomes 7q32, 3q28, 4q32, Xp22.3, Xp11.23-p11.22, 1p36 and 16p13, respectively. CLC1 is highly expressed in skeletal muscle. Mutations in the gene encoding CLC1 lead to myotonia, an inheritable disorder characterized by muscle stiffness and renal salt wasting. CLC2 is highly expressed in the epithelia of several organs including lung, which suggests CLC2 may be a possible therapeutic target for cystic fibrosis. CLC3 expression is particularly abundant in neuronal tissue, while CLC4 expression is evident in skeletal and cardiac muscle as well as brain. Mutations in the gene encoding CLC5 lead to Dent’s disease, a renal disorder characterized by proteinuria and hypercalciuria. CLC6 and CLC7 are broadly expressed in several tissues including testis, kidney, brain and muscle.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-10307R-CY5)
Fournisseur:
Bioss
Description:
The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport and maintain cellular volume. The genes encoding human CLC-1 through CLC-7 map to chromosomes 7q32, 3q28, 4q32, Xp22.3, Xp11.23-p11.22, 1p36 and 16p13, respectively. CLC1 is highly expressed in skeletal muscle. Mutations in the gene encoding CLC1 lead to myotonia, an inheritable disorder characterized by muscle stiffness and renal salt wasting. CLC2 is highly expressed in the epithelia of several organs including lung, which suggests CLC2 may be a possible therapeutic target for cystic fibrosis. CLC3 expression is particularly abundant in neuronal tissue, while CLC4 expression is evident in skeletal and cardiac muscle as well as brain. Mutations in the gene encoding CLC5 lead to Dent’s disease, a renal disorder characterized by proteinuria and hypercalciuria. CLC6 and CLC7 are broadly expressed in several tissues including testis, kidney, brain and muscle.
UOM:
1 * 100 µl
Fournisseur:
Serva
Description:
4-Methylumbelliferyl phosphate disodium salt (4-MUP-Na2)
Numéro de catalogue:
(J66414.03)
Fournisseur:
AAT BIOQUEST INC
Description:
JC-1 is widely used for determining mitochondrial membrane potential with flow cytometry.
Numéro de catalogue:
(PROOMM0253.00)
Fournisseur:
LGC Standards PROMOCHEM
Description:
Ampicilline sel de sodium
UOM:
1 * 500 mg
Numéro de catalogue:
(AATB20621)
Fournisseur:
AAT BIOQUEST INC
Description:
The cell-impermeant Fura-8FF is an analog of Fura-8 with much lower calcium binding affinity, Kd ~10 µM.
UOM:
1 * 500 µG
New Product
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