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Image Unavailable-77439-476

Anti-CA II Rabbit Polyclonal Antibody

Catalog Number: (77439-476)
Supplier: Bioss
Description: Essential for bone resorption and osteoclast differentiation (By similarity). Reversible hydration of carbon dioxide. Can hydrates cyanamide to urea. Involved in the regulation of fluid secretion into the anterior chamber of the eye.
Image Unavailable-TCE0095-025G

Ethylenediaminetetraacetic acid manganese disodium salt hydrate ≥95.0% (by titrimetric analysis)

Catalog Number: (TCE0095-025G)
Supplier: TCI America
Description: CAS Number: 15375-84-5
MDL Number: MFCD00054451
Molecular Formula: C10H16N2O8
Molecular Weight: 389.13
Purity/Analysis Method: >95.0% (T)
Form: Crystal

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Product Image-RC301032

Fehling's reagent I (copper(II) sulfate solution) for quantitative determination of reducing sugars

Supplier: Ricca Chemical
Description: Fehling Solution A. AOAC, EPA for determination of reducing sugars. Use with Fehling's Alkaline Solution, Group No.3000. Container: Cubitainer.

SDS Certificates Small Business Enterprise

Image Unavailable-10336-594

Anti-KCNJ11 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (10336-594)
Supplier: Bioss
Description: Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq]
Image Unavailable-CAAAAA12714-36

Barium hydroxide octahydrate 97%

Supplier: Thermo Scientific Chemicals
Description: Barium hydroxide octahydrate 97%

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Image Unavailable-76098-950

Anti-Kir6.2 (KCNJ11) Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (76098-950)
Supplier: Bioss
Description: Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. .
Image Unavailable-10336-600

Anti-KCNJ11 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (10336-600)
Supplier: Bioss
Description: Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq]
Image Unavailable-10336-592

Anti-KCNJ11 Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (10336-592)
Supplier: Bioss
Description: Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq]
Image Unavailable-TCC0373-025G

Cobalt(II) acetylacetonate dihydrate ≥97% (dried basis)

Supplier: TCI America
Description: CAS Number: 123334-29-2 MDL Number: MFCD00000014 Molecular Formula: C10H14CoO4 Molecular Weight: 257.15 Purity/Analysis Method: <gt/>98.0% (T) Form: Crystal

SDS

Image Unavailable-CA1.01737.0500

Barium hydroxide octahydrate, EMSURE® for analysis, Supelco®

Catalog Number: (CA1.01737.0500)
Supplier: MilliporeSigma
Description: Barium hydroxide octahydrate, EMSURE® for analysis, Supelco®

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Product Image-470300-624

Calcium Nitrate 4-Hydrate

Supplier: Ward's Science
Description: CAS Number: 13477-34-4
Formula Weight: 236.15
Formula: Ca(NO3)2·4H2O
Hazard Info: Flammable, Oxidizer, Explosive
Density (g/mL): 2.36
Boiling Point (°C): Decomposes
Freezing Point (°C): 45
Solubility: Water, Alcohol and Acetone
Synonyms: Calcium Nitrate Tetrahydrate, Nitric Acid Calcium(II) Salt
Shelf Life (months): 12
Storage: Yellow

SDS

Product Image-RC491016

Methylene blue solution II 0.05 mL (1 drop) = 0.1 mg/L Sulfide

Catalog Number: (RC491016)
Supplier: Ricca Chemical
Description: APHA , EPA for Sulfide. 0.05 mL (1 drop) = 0.1 mg/L Sulfide. Container: Glass.

SDS Certificates Small Business Enterprise


Image Unavailable-76098-952

Anti-Kir6.2 (KCNJ11) Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (76098-952)
Supplier: Bioss
Description: Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. .
Image Unavailable-10336-598

Anti-KCNJ11 Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (10336-598)
Supplier: Bioss
Description: Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq]
Image Unavailable-10336-922

Anti-KCNJ11 Rabbit Polyclonal Antibody

Catalog Number: (10336-922)
Supplier: Bioss
Description: Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq]
Image Unavailable-10336-596

Anti-KCNJ11 Rabbit Polyclonal Antibody (Cy5.5®)

Catalog Number: (10336-596)
Supplier: Bioss
Description: Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins and is found associated with the sulfonylurea receptor SUR. Mutations in this gene are a cause of familial persistent hyperinsulinemic hypoglycemia of infancy (PHHI), an autosomal recessive disorder characterized by unregulated insulin secretion. Defects in this gene may also contribute to autosomal dominant non-insulin-dependent diabetes mellitus type II (NIDDM), transient neonatal diabetes mellitus type 3 (TNDM3), and permanent neonatal diabetes mellitus (PNDM). Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq]
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