Print…

You Searched For: Pigment+Red+22


23 207  results were found

Refine Results Sort by
SearchResultCount:"23207"

Sort Results

List View Easy View (new)

Rate These Search Results

Image Unavailable-SIAL232033-100G

Titanium(IV) oxide anatase, Sigma-Aldrich®

Supplier: Merck
Description: Titanium(IV) oxide anatase, Sigma-Aldrich®

Image Unavailable-SIAL637262-100G

Titanium(IV) oxide rutile, Sigma-Aldrich®

Supplier: Merck
Description: Titanium(IV) oxide rutile, Sigma-Aldrich®

Image Unavailable-BOSSBS-12335R-A555

Anti-HFE Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Catalog Number: (BOSSBS-12335R-A555)
Supplier: Bioss
Description: The features of hemochromatosis include cirrhosis of the liver, diabetes, hypermelanotic pigmentation of the skin, and heart failure. Since hemochromatosis is a relatively easily treated disorder if diagnosed, this is a form of preventable cancer. The HFE protein, which is defective in hereditary hemo-chromatosis, normally is expressed in crypt enterocytes of the duodenum where it has a unique, predominantly intracellular localization. In placenta, the HFE protein co-localizes with and forms a stable association with the transferrin receptor (TfR), providing a link between the HFE protein and iron transport. Immunocytochemistry shows that the HFE protein and TfR both are expressed in the crypt enterocytes. Western blots show that, as is the case in human placenta, the HFE protein in crypt enterocytes is physically associated with the TfR and with β2-microglobulin. It is proposed that HFE has two mutually exclusive activities in cells: inhibition of uptake or inhibition of release of iron and that the balance between serum transferrin saturation and serum transferrin-receptor concentrations determines which of these functions predominates. The gene which encodes HFE maps to human chromosome 6p21.3.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-12335R-FITC

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

Catalog Number: (BOSSBS-12335R-FITC)
Supplier: Bioss
Description: The features of hemochromatosis include cirrhosis of the liver, diabetes, hypermelanotic pigmentation of the skin, and heart failure. Since hemochromatosis is a relatively easily treated disorder if diagnosed, this is a form of preventable cancer. The HFE protein, which is defective in hereditary hemo-chromatosis, normally is expressed in crypt enterocytes of the duodenum where it has a unique, predominantly intracellular localization. In placenta, the HFE protein co-localizes with and forms a stable association with the transferrin receptor (TfR), providing a link between the HFE protein and iron transport. Immunocytochemistry shows that the HFE protein and TfR both are expressed in the crypt enterocytes. Western blots show that, as is the case in human placenta, the HFE protein in crypt enterocytes is physically associated with the TfR and with β2-microglobulin. It is proposed that HFE has two mutually exclusive activities in cells: inhibition of uptake or inhibition of release of iron and that the balance between serum transferrin saturation and serum transferrin-receptor concentrations determines which of these functions predominates. The gene which encodes HFE maps to human chromosome 6p21.3.
UOM: 1 * 100 µl
Product Image-SIMEVF2122

Grindometers

Supplier: Industrial Physics
Description: These grindometers or gauges of fineness are precision instruments to determine particle size and fineness of many materials like paints, lacquers, pigments, filler, chocolate and more. TQC Grindometers have double grooves with graded slopes graduated in three different parameters: µm (microns), NS (Hegman) and PCU (North).

Image Unavailable-AMARL29000-GA/WC

High-Grade Precision Thermometers

Catalog Number: (AMARL29000-GA/WC)
Supplier: Amarell
Description: This high-grade precision thermometer features a solid stem, operates in the temperature range of −10 to +480 °C, has a white-backed. It is designed for total immersion, uses durable pigment, and is suitable for government verification.
UOM: 1 * 1 items

New Product


Product Image-PRSI25-378

Anti-VAX1 Rabbit Polyclonal Antibody

Catalog Number: (PRSI25-378)
Supplier: ProSci Inc.
Description: Vax1 is required for axon guidance and major tract formation in the developing forebrain. Vax1 may contribute to the differentiation of the neuroretina, pigmented epithelium and optic stalk.
UOM: 1 * 50 µG
Product Image-142-1953

Cleaning agent, TICKOPUR RW 77

Catalog Number: (142-1953)
Supplier: BANDELIN-ELECTRONIC
Description: Cleaning agent suitable for cleaning of ultrasonic bath. It can be used to clean glass, metal, ceramics, plastic, rubber and removes grease, oils, wax, protein, pigments, etc.
UOM: 1 * 2 L
Product Image-PRSI29-974

Anti-TYR Rabbit Polyclonal Antibody

Catalog Number: (PRSI29-974)
Supplier: ProSci Inc.
Description: TYR is a copper-containing oxidase that functions in the formation of pigments such as melanins and other polyphenolic compounds. It catalyzes the rate-limiting conversions of tyrosine to DOPA, DOPA to DOPA-quinone and possibly 5,6-dihydroxyindole to indole-5,6 quinone.
UOM: 1 * 100 µG
Image Unavailable-BOSSBS-12335R-CY5

Anti-HFE Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (BOSSBS-12335R-CY5)
Supplier: Bioss
Description: The features of hemochromatosis include cirrhosis of the liver, diabetes, hypermelanotic pigmentation of the skin, and heart failure. Since hemochromatosis is a relatively easily treated disorder if diagnosed, this is a form of preventable cancer. The HFE protein, which is defective in hereditary hemo-chromatosis, normally is expressed in crypt enterocytes of the duodenum where it has a unique, predominantly intracellular localization. In placenta, the HFE protein co-localizes with and forms a stable association with the transferrin receptor (TfR), providing a link between the HFE protein and iron transport. Immunocytochemistry shows that the HFE protein and TfR both are expressed in the crypt enterocytes. Western blots show that, as is the case in human placenta, the HFE protein in crypt enterocytes is physically associated with the TfR and with β2-microglobulin. It is proposed that HFE has two mutually exclusive activities in cells: inhibition of uptake or inhibition of release of iron and that the balance between serum transferrin saturation and serum transferrin-receptor concentrations determines which of these functions predominates. The gene which encodes HFE maps to human chromosome 6p21.3.
UOM: 1 * 100 µl
Image Unavailable-SIAL252980-100G

Copper(II) phthalocyanine 90% (dye content) β-form, Sigma-Aldrich®

Supplier: Merck
Description: Copper(II) phthalocyanine 90% (dye content) β-form, Sigma-Aldrich®

Product Image-PRSI29-636

Anti-STK11 Rabbit Polyclonal Antibody

Catalog Number: (PRSI29-636)
Supplier: ProSci Inc.
Description: STK11is a member of the serine/threonine kinase family, regulates cell polarity and functions as a tumor suppressor. Mutations in its gene have been associated with Peutz-Jeghers syndrome, an autosomal dominant disorder characterized by the growth of polyps in the gastrointestinal tract, pigmented macules on the skin and mouth, and other neoplasms.This gene, which encodes a member of the serine/threonine kinase family, regulates cell polarity and functions as a tumor suppressor. Mutations in this gene have been associated with Peutz-Jeghers syndrome, an autosomal dominant disorder characterized by the growth of polyps in the gastrointestinal tract, pigmented macules on the skin and mouth, and other neoplasms. Alternate transcriptional splice variants of this gene have been observed but have not been thoroughly characterized.
UOM: 1 * 100 µG
Image Unavailable-BOSSBS-12335R-A647

Anti-HFE Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalog Number: (BOSSBS-12335R-A647)
Supplier: Bioss
Description: The features of hemochromatosis include cirrhosis of the liver, diabetes, hypermelanotic pigmentation of the skin, and heart failure. Since hemochromatosis is a relatively easily treated disorder if diagnosed, this is a form of preventable cancer. The HFE protein, which is defective in hereditary hemo-chromatosis, normally is expressed in crypt enterocytes of the duodenum where it has a unique, predominantly intracellular localization. In placenta, the HFE protein co-localizes with and forms a stable association with the transferrin receptor (TfR), providing a link between the HFE protein and iron transport. Immunocytochemistry shows that the HFE protein and TfR both are expressed in the crypt enterocytes. Western blots show that, as is the case in human placenta, the HFE protein in crypt enterocytes is physically associated with the TfR and with β2-microglobulin. It is proposed that HFE has two mutually exclusive activities in cells: inhibition of uptake or inhibition of release of iron and that the balance between serum transferrin saturation and serum transferrin-receptor concentrations determines which of these functions predominates. The gene which encodes HFE maps to human chromosome 6p21.3.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-12335R-A680

Anti-HFE/Hemochromatosis Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (BOSSBS-12335R-A680)
Supplier: Bioss
Description: The features of hemochromatosis include cirrhosis of the liver, diabetes, hypermelanotic pigmentation of the skin, and heart failure. Since hemochromatosis is a relatively easily treated disorder if diagnosed, this is a form of preventable cancer. The HFE protein, which is defective in hereditary hemo-chromatosis, normally is expressed in crypt enterocytes of the duodenum where it has a unique, predominantly intracellular localisation. In placenta, the HFE protein co-localizes with and forms a stable association with the transferrin receptor (TfR), providing a link between the HFE protein and iron transport. Immunocytochemistry shows that the HFE protein and TfR both are expressed in the crypt enterocytes. Western blots show that, as is the case in human placenta, the HFE protein in crypt enterocytes is physically associated with the TfR and with 2-microglobulin. It is proposed that HFE has two mutually exclusive activities in cells: inhibition of uptake or inhibition of release of iron and that the balance between serum transferrin saturation and serum transferrin-receptor concentrations determines which of these functions predominates. The gene which encodes HFE maps to human chromosome 6p21.3.
UOM: 1 * 100 µl
Product Image-FAWE13632-003

Protective hand creams, Physioderm®, SANSIBAL®

Catalog Number: (FAWE13632-003)
Supplier: FAWECO HAUTSCHUTZ
Description: The water-soluble, pigment-based emulsion develops a separating and a protective film. This solid grid effectively prevents water-insoluble hazards from penetrating the upper layers of the skin. The protective film also reduces the adherence of dirt.
UOM: 1 * 12 items
Product Image-113-02245

Overalls with Bib and Braces, Fristads® PR54-22, Design B, Royal Blue

Supplier: FRISTADS KANSAS
Description: Overalls made from 65% polyester and 35% cotton, with soft nap on reverse side.

Inquire for Price
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at +43 1 97002 - 0.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at +43 1 97002 - 0.
Dual use goods can only be delivered within the European Union.
Dual use goods can only be delivered within the European Union.
This product has been blocked by your organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at +43 1 97002 - 0.
465 - 480 of 23 207
no targeter for Bottom