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Product Image-217-9445

Stoppers, rubber, conical

Catalog Number: (217-9445)
Supplier: DEUTSCH NEUMANN
Description: Natural rubber, grey.
UOM: 1 * 5 items
Image Unavailable-BOSSBS-2700R-A350

Anti-CK10 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Catalog Number: (BOSSBS-2700R-A350)
Supplier: Bioss
Description: Cytokeratin 10 is a heterotetramer of two type I and two type II keratins. Cytokeratin 10 is generally associated with keratin 1. It is seen in all suprabasal cell layers including stratum corneum. A number of alleles are known that mainly differ in the Gly-rich region (positions 490-560). Defects in cytokeratin 10 are a cause of epidermolytic hyperkeratosis (EHK), also known as bullous congenital ichthyosiform erythroderma (BCIE) or bullous erythroderma ichthyosiformis congenita of Brocq. EHK is an hereditary skin disorder characterized by blistering and a marked thickening of the stratum corneum. At birth, affected individuals usually present with redness, blisters and superficial erosions due to cytolysis. Within a few weeks, the erythroderma and blister formation diminish and hyperkeratoses develop. Transmission is autosomal dominant, but most cases are sporadic. Defects in cytokeratin 10 are also a cause of annular epidermolytic ichthyosis (AEI), also known as cyclic ichthyosis with epidermolytic hyperkeratosis. AEI resembles clinical and histologic features of both epidermolytic hyperkeratosis and ichthyosis bullosa of Siemens.
UOM: 1 * 100 µl
Product Image-HECH92159111490

Rubber Stoppers

Supplier: GLASWARENFABRIK KARL HECHT
Description: DIN 12871, made of natural rubber, hardness 40 Shore A.

Image Unavailable-BOSSBS-2700R-CY3

Anti-CK10 Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (BOSSBS-2700R-CY3)
Supplier: Bioss
Description: Cytokeratin 10 is a heterotetramer of two type I and two type II keratins. Cytokeratin 10 is generally associated with keratin 1. It is seen in all suprabasal cell layers including stratum corneum. A number of alleles are known that mainly differ in the Gly-rich region (positions 490-560). Defects in cytokeratin 10 are a cause of epidermolytic hyperkeratosis (EHK), also known as bullous congenital ichthyosiform erythroderma (BCIE) or bullous erythroderma ichthyosiformis congenita of Brocq. EHK is an hereditary skin disorder characterized by blistering and a marked thickening of the stratum corneum. At birth, affected individuals usually present with redness, blisters and superficial erosions due to cytolysis. Within a few weeks, the erythroderma and blister formation diminish and hyperkeratoses develop. Transmission is autosomal dominant, but most cases are sporadic. Defects in cytokeratin 10 are also a cause of annular epidermolytic ichthyosis (AEI), also known as cyclic ichthyosis with epidermolytic hyperkeratosis. AEI resembles clinical and histologic features of both epidermolytic hyperkeratosis and ichthyosis bullosa of Siemens.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-2700R-A647

Anti-CK10 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalog Number: (BOSSBS-2700R-A647)
Supplier: Bioss
Description: Cytokeratin 10 is a heterotetramer of two type I and two type II keratins. Cytokeratin 10 is generally associated with keratin 1. It is seen in all suprabasal cell layers including stratum corneum. A number of alleles are known that mainly differ in the Gly-rich region (positions 490-560). Defects in cytokeratin 10 are a cause of epidermolytic hyperkeratosis (EHK), also known as bullous congenital ichthyosiform erythroderma (BCIE) or bullous erythroderma ichthyosiformis congenita of Brocq. EHK is an hereditary skin disorder characterized by blistering and a marked thickening of the stratum corneum. At birth, affected individuals usually present with redness, blisters and superficial erosions due to cytolysis. Within a few weeks, the erythroderma and blister formation diminish and hyperkeratoses develop. Transmission is autosomal dominant, but most cases are sporadic. Defects in cytokeratin 10 are also a cause of annular epidermolytic ichthyosis (AEI), also known as cyclic ichthyosis with epidermolytic hyperkeratosis. AEI resembles clinical and histologic features of both epidermolytic hyperkeratosis and ichthyosis bullosa of Siemens.
UOM: 1 * 100 µl
Product Image-217-9722

Silicone foam stoppers, conical

Catalog Number: (217-9722)
Supplier: KOEHLER TECHNISCHE PRODUKTEN
Description: These coloured conical stoppers are made from silicone foam.
UOM: 1 * 1 items
Image Unavailable-1.01517.2500

Silver sulphate 10 g/l in sulphuric acid for COD determination, Supelco®

Supplier: Merck
Description: Silver sulphate 10 g/l in sulphuric acid for COD determination, Supelco®

MSDS Certificates Sale

Image Unavailable-05495-25G

Silver Protein

Supplier: SIGMA ALDRICH MICROSCOPY
Description: Protargol silver impregnation and neuronal selectivity for light and electron microscopic observations.

Image Unavailable-BOSSBS-2700R-CY5.5

Anti-CK10 Rabbit Polyclonal Antibody (Cy5.5®)

Catalog Number: (BOSSBS-2700R-CY5.5)
Supplier: Bioss
Description: Cytokeratin 10 is a heterotetramer of two type I and two type II keratins. Cytokeratin 10 is generally associated with keratin 1. It is seen in all suprabasal cell layers including stratum corneum. A number of alleles are known that mainly differ in the Gly-rich region (positions 490-560). Defects in cytokeratin 10 are a cause of epidermolytic hyperkeratosis (EHK), also known as bullous congenital ichthyosiform erythroderma (BCIE) or bullous erythroderma ichthyosiformis congenita of Brocq. EHK is an hereditary skin disorder characterized by blistering and a marked thickening of the stratum corneum. At birth, affected individuals usually present with redness, blisters and superficial erosions due to cytolysis. Within a few weeks, the erythroderma and blister formation diminish and hyperkeratoses develop. Transmission is autosomal dominant, but most cases are sporadic. Defects in cytokeratin 10 are also a cause of annular epidermolytic ichthyosis (AEI), also known as cyclic ichthyosis with epidermolytic hyperkeratosis. AEI resembles clinical and histologic features of both epidermolytic hyperkeratosis and ichthyosis bullosa of Siemens.
UOM: 1 * 100 µl
Product Image-525.54000.00

Pump tubing, Viton®

Catalog Number: (525.54000.00)
Supplier: Heidolph Instruments GmbH & Co.KG
Description: Fluorocarbon rubber, thermoformed Viton B (67% fluorinated), opaque black.
UOM: 1 * 1 m
Image Unavailable-BOSSBS-2700R-A555

Anti-CK10 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Catalog Number: (BOSSBS-2700R-A555)
Supplier: Bioss
Description: Cytokeratin 10 is a heterotetramer of two type I and two type II keratins. Cytokeratin 10 is generally associated with keratin 1. It is seen in all suprabasal cell layers including stratum corneum. A number of alleles are known that mainly differ in the Gly-rich region (positions 490-560). Defects in cytokeratin 10 are a cause of epidermolytic hyperkeratosis (EHK), also known as bullous congenital ichthyosiform erythroderma (BCIE) or bullous erythroderma ichthyosiformis congenita of Brocq. EHK is an hereditary skin disorder characterized by blistering and a marked thickening of the stratum corneum. At birth, affected individuals usually present with redness, blisters and superficial erosions due to cytolysis. Within a few weeks, the erythroderma and blister formation diminish and hyperkeratoses develop. Transmission is autosomal dominant, but most cases are sporadic. Defects in cytokeratin 10 are also a cause of annular epidermolytic ichthyosis (AEI), also known as cyclic ichthyosis with epidermolytic hyperkeratosis. AEI resembles clinical and histologic features of both epidermolytic hyperkeratosis and ichthyosis bullosa of Siemens.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-2700R-HRP

Anti-CK10 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (BOSSBS-2700R-HRP)
Supplier: Bioss
Description: Cytokeratin 10 is a heterotetramer of two type I and two type II keratins. Cytokeratin 10 is generally associated with keratin 1. It is seen in all suprabasal cell layers including stratum corneum. A number of alleles are known that mainly differ in the Gly-rich region (positions 490-560). Defects in cytokeratin 10 are a cause of epidermolytic hyperkeratosis (EHK), also known as bullous congenital ichthyosiform erythroderma (BCIE) or bullous erythroderma ichthyosiformis congenita of Brocq. EHK is an hereditary skin disorder characterized by blistering and a marked thickening of the stratum corneum. At birth, affected individuals usually present with redness, blisters and superficial erosions due to cytolysis. Within a few weeks, the erythroderma and blister formation diminish and hyperkeratoses develop. Transmission is autosomal dominant, but most cases are sporadic. Defects in cytokeratin 10 are also a cause of annular epidermolytic ichthyosis (AEI), also known as cyclic ichthyosis with epidermolytic hyperkeratosis. AEI resembles clinical and histologic features of both epidermolytic hyperkeratosis and ichthyosis bullosa of Siemens.
UOM: 1 * 100 µl
Product Image-SOCO3210.3049

Qualitix® Sterilisation Pouches

Catalog Number: (SOCO3210.3049)
Supplier: Socorex Isba
Description: Fitting any small to mid-size laboratory, medical, dental or veterinary device, the Qualitix® single use pouches provide easy and effective wrapping of items requiring sterilization.
UOM: 1 * 200 items

New Product


Product Image-21589.233

Silver sulphate ≥98%, TECHNICAL

Supplier: VWR Chemicals
Description: Silver sulphate ≥98%, TECHNICAL

MSDS Certificates

Image Unavailable-ROTHKE63.1

Pipette brushes, Rotilabo®

Catalog Number: (ROTHKE63.1)
Supplier: Roth Carl
Description: Pipette brushes with uncoloured natural bristles.
UOM: 1 * 5 items

Market Source Item This is a MarketSource item. Additional charges may apply

Image Unavailable-1.01509.0100

Silver sulphate ACS analytical reagent, Supelco®

Supplier: Merck
Description: Silver sulphate ACS analytical reagent, Supelco®

MSDS

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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 on +353 1 88 22222.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at eurega_services@eu.vwr.com
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This product has been blocked by your organisation. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
Product(s) marked with this symbol are discontinued - sold till end of stock. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service on +353 1 8822222.
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