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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]
Image Unavailable-10339-588

Anti-KCNJ11 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (10339-588)
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-CAPIPA5-18710

Anti-KCNJ11 Goat Polyclonal Antibody

Catalog Number: (CAPIPA5-18710)
Supplier: Thermo Scientific
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 , 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 , transient neonatal diabetes mellitus type 3 , and permanent neonatal diabetes mellitus . Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene.
Image Unavailable-CAPIPA5-18711

Anti-KCNJ11 Goat Polyclonal Antibody

Catalog Number: (CAPIPA5-18711)
Supplier: Thermo Scientific
Description: This antibody is predicted to react with canine, mouse and rat based on sequence homology. 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 , 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 , transient neonatal diabetes mellitus type 3 , and permanent neonatal diabetes mellitus . Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene.
Image Unavailable-CAAA14499-30

Barium hydroxide octahydrate 98+% ACS

Supplier: Thermo Scientific Chemicals
Description: Used in manufacture of alkali, glass; in synthetic rubber vulcanization, alkalizing agent in water softening, boiler scale remedy, softening water

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Image Unavailable-10083-916

Anti-CA2 Rabbit Polyclonal Antibody

Catalog Number: (10083-916)
Supplier: Proteintech
Description: CA2(carbonic anhydrase II ) is also named as Car2, CA-II, CAII and belongs to the alpha-carbonic anhydrase family. It reversibly hydrates CO2 in cellular ion transport and homeostasis. CA2 is essential for bone resorption and osteoclast differentiation. It regulates SLC9A1 activity via a phosphorylation-regulated CAII binding site in SLC9A1 tail. It also may be involved in the development of brain. Defects in CA2 are the cause of osteopetrosis autosomal recessive type 3 (OPTB3).
Product Image-CARL200401136S

Anti-CA2 Rabbit Polyclonal Antibody

Catalog Number: (CARL200401136S)
Supplier: Rockland Immunochemical
Description: Carbonic Anhydrase II Antibody is suitable for western blotting, ELISA and IHC. Researchers should determine optimal titers for applications that are not stated below.
Image Unavailable-CAAA20129-14

Cadmium chloride hydrate ≥99.99% (metals basis)

Supplier: Thermo Scientific Chemicals
Description: MDL: MFCD00149627

Certificates

Image Unavailable-CAAAA10276-0B

Iron(III) citrate hydrate Fe(III) 16.5-20% (Fe(II) ≤ 5%)

Supplier: Thermo Scientific Chemicals
Description: Provides a source of iron used in cell culture applications. Provides iron in a less toxic form than free iron salts.

Certificates

Product Image-470300-772

Cobalt(II) Nitrate Hexahydrate

Supplier: Ward's Science
Description: CAS Number: 10026-22-9
Formula Weight: 291.03
Formula: Co(NO3)2·6H2O
Hazard Info: Oxidizer
Density (g/mL): 1.88
Freezing Point (°C): 55
Solubility: Most Organic Solvents
Synonyms: Cobalt Nitrate Hexahydrate, Cobaltous Nitrate Hexahydrate
Shelf Life (months): 36
Storage: Yellow

SDS

Image Unavailable-CAAA10661-09

Cadmium chloride hydrate ≥99.998% (metals basis), Puratronic®

Supplier: Thermo Scientific Chemicals
Description: MDL: MFCD00149627

Certificates

Image Unavailable-CAPIPA5-18377

Anti-DPP10 Goat Polyclonal Antibody

Catalog Number: (CAPIPA5-18377)
Supplier: Thermo Scientific
Description: This antibody is predicted to react with bovine and canine based on sequence homology. This gene encodes a single-pass type II membrane protein that is a member of the S9B family in clan SC of the serine proteases. This protein has no detectable protease activity, most likely due to the absence of the conserved serine residue normally present in the catalytic domain of serine proteases. However, it does bind specific voltage-gated potassium channels and alters their expression and biophysical properties. Mutations in this gene have been associated with asthma. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.
Image Unavailable-10480-128

Anti-CA11 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (10480-128)
Supplier: Bioss
Description: Carbonic anhydrases (CAs) are members of a large family of zinc metalloenzymes responsible for catalyzing the reversible hydration of carbon dioxide. CAs show extensive diversity in their distribution and subcellular localization. They are involved in a variety of biological processes, including calcification, bone resorption, respiration, acid-base balance and the formation of aqueous humor, saliva, gastric juice and cerebrospinal fluid. CA XI, also referred to as carbonic anhydrase-related protein 11 precursor (CA-RP XI) or carbonic anhydrase-related protein 2 (CA-RP II), is a member of the carbonic anhydrase family that lacks two of the three Zn-binding motifs essential for carbonic anhydrase activity. For this reason, CA XI does not exhibit catalytic activity. It is expressed primarily in brain but is also found in spinal cord and thyroid. CA XI may play a role in brain development.Tissue specificity:Expressed abundantly in the brain with moderate expression also present in spinal cord and thyroid.
Image Unavailable-10480-120

Anti-CA11 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (10480-120)
Supplier: Bioss
Description: Carbonic anhydrases (CAs) are members of a large family of zinc metalloenzymes responsible for catalyzing the reversible hydration of carbon dioxide. CAs show extensive diversity in their distribution and subcellular localization. They are involved in a variety of biological processes, including calcification, bone resorption, respiration, acid-base balance and the formation of aqueous humor, saliva, gastric juice and cerebrospinal fluid. CA XI, also referred to as carbonic anhydrase-related protein 11 precursor (CA-RP XI) or carbonic anhydrase-related protein 2 (CA-RP II), is a member of the carbonic anhydrase family that lacks two of the three Zn-binding motifs essential for carbonic anhydrase activity. For this reason, CA XI does not exhibit catalytic activity. It is expressed primarily in brain but is also found in spinal cord and thyroid. CA XI may play a role in brain development.Tissue specificity:Expressed abundantly in the brain with moderate expression also present in spinal cord and thyroid.
Image Unavailable-10480-106

Anti-CA11 Rabbit Polyclonal Antibody

Catalog Number: (10480-106)
Supplier: Bioss
Description: Carbonic anhydrases (CAs) are members of a large family of zinc metalloenzymes responsible for catalyzing the reversible hydration of carbon dioxide. CAs show extensive diversity in their distribution and subcellular localization. They are involved in a variety of biological processes, including calcification, bone resorption, respiration, acid-base balance and the formation of aqueous humor, saliva, gastric juice and cerebrospinal fluid. CA XI, also referred to as carbonic anhydrase-related protein 11 precursor (CA-RP XI) or carbonic anhydrase-related protein 2 (CA-RP II), is a member of the carbonic anhydrase family that lacks two of the three Zn-binding motifs essential for carbonic anhydrase activity. For this reason, CA XI does not exhibit catalytic activity. It is expressed primarily in brain but is also found in spinal cord and thyroid. CA XI may play a role in brain development.Tissue specificity:Expressed abundantly in the brain with moderate expression also present in spinal cord and thyroid.
Image Unavailable-10480-126

Anti-CA11 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (10480-126)
Supplier: Bioss
Description: Carbonic anhydrases (CAs) are members of a large family of zinc metalloenzymes responsible for catalyzing the reversible hydration of carbon dioxide. CAs show extensive diversity in their distribution and subcellular localization. They are involved in a variety of biological processes, including calcification, bone resorption, respiration, acid-base balance and the formation of aqueous humor, saliva, gastric juice and cerebrospinal fluid. CA XI, also referred to as carbonic anhydrase-related protein 11 precursor (CA-RP XI) or carbonic anhydrase-related protein 2 (CA-RP II), is a member of the carbonic anhydrase family that lacks two of the three Zn-binding motifs essential for carbonic anhydrase activity. For this reason, CA XI does not exhibit catalytic activity. It is expressed primarily in brain but is also found in spinal cord and thyroid. CA XI may play a role in brain development.Tissue specificity:Expressed abundantly in the brain with moderate expression also present in spinal cord and thyroid.
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