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Image Unavailable-BOSSBS-6007R-CY3

Anti-FLCN Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (BOSSBS-6007R-CY3)
Supplier: Bioss
Description: This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of this gene results in three transcript variants encoding different isoforms.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-6007R-CY7

Anti-FLCN Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (BOSSBS-6007R-CY7)
Supplier: Bioss
Description: This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of this gene results in three transcript variants encoding different isoforms.
UOM: 1 * 100 µl
Product Image-MFLX30526-16BLK

Smiths Medical® Luer Fittings on PVC Flexible Tubing, Straight

Supplier: Avantor Fluid Handling
Description: Get a seamless transition from source to system.

Image Unavailable-BOSSBS-13000R-A555

Anti-DHRS7B Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Catalog Number: (BOSSBS-13000R-A555)
Supplier: Bioss
Description: This gene is located within the Smith-Magenis syndrome region on chromosome 17. It encodes a protein of unknown function. [provided by RefSeq, Jul 2008].
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13000R-CY3

Anti-DHRS7B Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (BOSSBS-13000R-CY3)
Supplier: Bioss
Description: This gene is located within the Smith-Magenis syndrome region on chromosome 17. It encodes a protein of unknown function. [provided by RefSeq, Jul 2008].
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13000R-A647

Anti-DHRS7B Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Catalog Number: (BOSSBS-13000R-A647)
Supplier: Bioss
Description: This gene is located within the Smith-Magenis syndrome region on chromosome 17. It encodes a protein of unknown function. [provided by RefSeq, Jul 2008].
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13000R-HRP

Anti-DHRS7B Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (BOSSBS-13000R-HRP)
Supplier: Bioss
Description: This gene is located within the Smith-Magenis syndrome region on chromosome 17. It encodes a protein of unknown function. [provided by RefSeq, Jul 2008].
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13000R-A680

Anti-DHRS7B Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (BOSSBS-13000R-A680)
Supplier: Bioss
Description: This gene is located within the Smith-Magenis syndrome region on chromosome 17. It encodes a protein of unknown function.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13000R-A350

Anti-DHRS7B Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Catalog Number: (BOSSBS-13000R-A350)
Supplier: Bioss
Description: This gene is located within the Smith-Magenis syndrome region on chromosome 17. It encodes a protein of unknown function. [provided by RefSeq, Jul 2008].
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-6007R

Anti-Folliculin Rabbit Polyclonal Antibody

Catalog Number: (BOSSBS-6007R)
Supplier: Bioss
Description: This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of this gene results in three transcript variants encoding different isoforms.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8719R-A488

Anti-LRP130 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Catalog Number: (BOSSBS-8719R-A488)
Supplier: Bioss
Description: Leucine-rich protein (LRP130) is a cytoplasmic mRNA-binding protein likely to be involved in the processing of mitochondrial DNA transcripts. Defects in the LRPPRC gene that encodes LRP130 result in the French-Canadian type of Leigh syndrome, a severe neurological disorder characterized by lesions in the subcortical region of the brain. LRP130 also interacts with the low-affinity receptor for leukemia inhibitory factor to produce an intracelluar signal cascade.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-8719R-FITC

Anti-LRP130 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (BOSSBS-8719R-FITC)
Supplier: Bioss
Description: Leucine-rich protein (LRP130) is a cytoplasmic mRNA-binding protein likely to be involved in the processing of mitochondrial DNA transcripts. Defects in the LRPPRC gene that encodes LRP130 result in the French-Canadian type of Leigh syndrome, a severe neurological disorder characterized by lesions in the subcortical region of the brain. LRP130 also interacts with the low-affinity receptor for leukemia inhibitory factor to produce an intracelluar signal cascade.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-6007R-A350

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

Catalog Number: (BOSSBS-6007R-A350)
Supplier: Bioss
Description: This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of this gene results in three transcript variants encoding different isoforms.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-6007R-FITC

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

Catalog Number: (BOSSBS-6007R-FITC)
Supplier: Bioss
Description: This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of this gene results in three transcript variants encoding different isoforms.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-6007R-CY5

Anti-FLCN Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (BOSSBS-6007R-CY5)
Supplier: Bioss
Description: This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of this gene results in three transcript variants encoding different isoforms.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-6007R-HRP

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

Catalog Number: (BOSSBS-6007R-HRP)
Supplier: Bioss
Description: This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of this gene results in three transcript variants encoding different isoforms.
UOM: 1 * 100 µl
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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
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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 on +353 1 88 22222.
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