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AG-1288 ≥98% (by TLC)

Catalog Number: (ENZOBMLEI3350050)
Supplier: ENZO LIFE SCIENCES
Description: Tyrosine kinase inhibitor. It has been shown to block TNFα induced cytotoxicity and to block glucocorticoid-induced COX-2 activity in human amnion cells (IC50=21μM). It is also reported to inhibit guanylyl cyclase.
UOM: 1 * 50 mg
Product Image-GPCIGI033Y

Folding sack truck

Catalog Number: (GPCIGI033Y)
Supplier: GPC Industries Ltd
Description: The folding sack trucks are made of aluminium, can be folded and unfolded easily and hence ideal for storing and transporting in confined spaces.
UOM: 1 * 1 items
Image Unavailable-BOSSBS-9563R-A555

Anti-LMBR1 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Catalog Number: (BOSSBS-9563R-A555)
Supplier: Bioss
Description: LMBR1 is a 490 amino acid multi-pass membrane protein that is widely expressed with strongest expression in heart and pancreas. Belonging to the LIMR family, LMBR1 shares 95% sequence identity with the mouse protein and may play crucial role in the evolution of limb and skeletal system. LMBR1 is critical for expression of sonic hedgehog (Shh) in the developing posterior limb bud mesenchyme. Mutations in the gene encoding LMBR1 is the cause of several rare conditions such as acheiropody (ACHP) and syndactyly type 4 (SDYT4). ACHP is an autosomal recessive inherited disorder characterized by bilateral congenital amputations of the hands and feet. LMBR1L (limb region 1 protein homolog-like), also known as LIMR (Lipocalin-1-interacting membrane receptor), is a 489 amino acid multi-pass membrane protein that is thought to act as a receptor for Lipocalin-1 and may also assist in its endocytosis.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9563R-CY5.5

Anti-LMBR1 Rabbit Polyclonal Antibody (Cy5.5®)

Catalog Number: (BOSSBS-9563R-CY5.5)
Supplier: Bioss
Description: LMBR1 is a 490 amino acid multi-pass membrane protein that is widely expressed with strongest expression in heart and pancreas. Belonging to the LIMR family, LMBR1 shares 95% sequence identity with the mouse protein and may play crucial role in the evolution of limb and skeletal system. LMBR1 is critical for expression of sonic hedgehog (Shh) in the developing posterior limb bud mesenchyme. Mutations in the gene encoding LMBR1 is the cause of several rare conditions such as acheiropody (ACHP) and syndactyly type 4 (SDYT4). ACHP is an autosomal recessive inherited disorder characterized by bilateral congenital amputations of the hands and feet. LMBR1L (limb region 1 protein homolog-like), also known as LIMR (Lipocalin-1-interacting membrane receptor), is a 489 amino acid multi-pass membrane protein that is thought to act as a receptor for Lipocalin-1 and may also assist in its endocytosis.
UOM: 1 * 100 µl
Product Image-SAMPA674-490

Instrument trays

Catalog Number: (SAMPA674-490)
Supplier: Sampling Systems
Description: Made from 304 stainless steel.
UOM: 1 * 1 items
Image Unavailable-BOSSBS-9563R-FITC

Anti-LMBR1 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (BOSSBS-9563R-FITC)
Supplier: Bioss
Description: LMBR1 is a 490 amino acid multi-pass membrane protein that is widely expressed with strongest expression in heart and pancreas. Belonging to the LIMR family, LMBR1 shares 95% sequence identity with the mouse protein and may play crucial role in the evolution of limb and skeletal system. LMBR1 is critical for expression of sonic hedgehog (Shh) in the developing posterior limb bud mesenchyme. Mutations in the gene encoding LMBR1 is the cause of several rare conditions such as acheiropody (ACHP) and syndactyly type 4 (SDYT4). ACHP is an autosomal recessive inherited disorder characterized by bilateral congenital amputations of the hands and feet. LMBR1L (limb region 1 protein homolog-like), also known as LIMR (Lipocalin-1-interacting membrane receptor), is a 489 amino acid multi-pass membrane protein that is thought to act as a receptor for Lipocalin-1 and may also assist in its endocytosis.
UOM: 1 * 100 µl
Product Image-21584.134

Silver(I) oxide ≥99%, TECHNICAL

Catalog Number: (21584.134)
Supplier: VWR Chemicals
Description: Silver(I) oxide ≥99%, TECHNICAL
UOM: 1 * 25 g

MSDS Certificates


Product Image-461-0918

Heating circulators, CORIO™ CD-BC series

Catalog Number: (461-0918)
Supplier: JULABO GmbH
Description: The powerful and robust CORIO™ laboratory circulators provide the exact temperature, absolute precision, and a wide working temperature range. The CORIO™ CD model is an advanced unit with professional technology for demanding applications and can be used for temperature control of internal or external applications. The jet nozzle allows continuous adjustment of the pump stream in the system. The insulated stainless steel baths are durable and have an integrated drain tap. These heating circulators are optimised for external temperature applications in combination with jacketed reactors, distillation apparatus, mini-plant applications, photometers, refractometers and can also be used for internal temperature applications of samples and small objects.
UOM: 1 * 1 items
Image Unavailable-BOSSBS-9563R-A750

Anti-D14 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (BOSSBS-9563R-A750)
Supplier: Bioss
Description: LMBR1 is a 490 amino acid multi-pass membrane protein that is widely expressed with strongest expression in heart and pancreas. Belonging to the LIMR family, LMBR1 shares 95% sequence identity with the mouse protein and may play crucial role in the evolution of limb and skeletal system. LMBR1 is critical for expression of sonic hedgehog (Shh) in the developing posterior limb bud mesenchyme. Mutations in the gene encoding LMBR1 is the cause of several rare conditions such as acheiropody (ACHP) and syndactyly type 4 (SDYT4). ACHP is an autosomal recessive inherited disorder characterised by bilateral congenital amputations of the hands and feet. LMBR1L (limb region 1 protein homolog-like), also known as LIMR (Lipocalin-1-interacting membrane receptor), is a 489 amino acid multi-pass membrane protein that is thought to act as a receptor for Lipocalin-1 and may also assist in its endocytosis.
UOM: 1 * 100 µl
Product Image-MMME490

Dual auto-reader for steam and vaporised hydrogen peroxide 490, Attest™

Catalog Number: (MMME490)
Supplier: 3M MEDICAL
Description: Auto-reader for use with 3M™ Attest™ Rapid Readout Biological Indicators and process challenge packs for steam. Includes ethernet cable for web app connectivity.
UOM: 1 * 1 items
Image Unavailable-1.01534.0050

Silver sulphate, Supelco®

Supplier: Merck
Description: Silver sulphate, Supelco®

MSDS

Image Unavailable-BOSSBS-9563R-A647

Anti-LMBR1 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalog Number: (BOSSBS-9563R-A647)
Supplier: Bioss
Description: LMBR1 is a 490 amino acid multi-pass membrane protein that is widely expressed with strongest expression in heart and pancreas. Belonging to the LIMR family, LMBR1 shares 95% sequence identity with the mouse protein and may play crucial role in the evolution of limb and skeletal system. LMBR1 is critical for expression of sonic hedgehog (Shh) in the developing posterior limb bud mesenchyme. Mutations in the gene encoding LMBR1 is the cause of several rare conditions such as acheiropody (ACHP) and syndactyly type 4 (SDYT4). ACHP is an autosomal recessive inherited disorder characterized by bilateral congenital amputations of the hands and feet. LMBR1L (limb region 1 protein homolog-like), also known as LIMR (Lipocalin-1-interacting membrane receptor), is a 489 amino acid multi-pass membrane protein that is thought to act as a receptor for Lipocalin-1 and may also assist in its endocytosis.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9563R

Anti-LMBR1 Rabbit Polyclonal Antibody

Catalog Number: (BOSSBS-9563R)
Supplier: Bioss
Description: LMBR1 is a 490 amino acid multi-pass membrane protein that is widely expressed with strongest expression in heart and pancreas. Belonging to the LIMR family, LMBR1 shares 95% sequence identity with the mouse protein and may play crucial role in the evolution of limb and skeletal system. LMBR1 is critical for expression of sonic hedgehog (Shh) in the developing posterior limb bud mesenchyme. Mutations in the gene encoding LMBR1 is the cause of several rare conditions such as acheiropody (ACHP) and syndactyly type 4 (SDYT4). ACHP is an autosomal recessive inherited disorder characterized by bilateral congenital amputations of the hands and feet. LMBR1L (limb region 1 protein homolog-like), also known as LIMR (Lipocalin-1-interacting membrane receptor), is a 489 amino acid multi-pass membrane protein that is thought to act as a receptor for Lipocalin-1 and may also assist in its endocytosis.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-2700R-CY5

Anti-CK10 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (BOSSBS-2700R-CY5)
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-A750

Anti-Cytokeratin 10 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (BOSSBS-2700R-A750)
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 characterised 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.

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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.
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
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
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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