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Image Unavailable-BOSSBS-15222R-CY7

Anti-C6ORF145 Rabbit Polyclonal Antibody (Cy7)

Catalog Number: (BOSSBS-15222R-CY7)
Supplier: Bioss
Description: Making up nearly 6% of the human genome, chromosome 6 contains around 1200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf145 gene product has been provisionally designated C6orf145 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15255R-FITC

Anti-C6ORF97 Rabbit Polyclonal Antibody (FITC)

Catalog Number: (BOSSBS-15255R-FITC)
Supplier: Bioss
Description: Making up nearly 6% of the human genome, chromosome 6 contains around 1200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf97 gene product has been provisionally designated C6orf97 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15249R-CY5

Anti-C6ORF57 Rabbit Polyclonal Antibody (Cy5)

Catalog Number: (BOSSBS-15249R-CY5)
Supplier: Bioss
Description: Making up nearly 6% of the human genome, chromosome 6 contains around 1200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf57 gene product has been provisionally designated C6orf57 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15218R-CY3

Anti-C6ORF132 Rabbit Polyclonal Antibody (Cy3)

Catalog Number: (BOSSBS-15218R-CY3)
Supplier: Bioss
Description: Making up nearly 6% of the human genome, chromosome 6 contains around 1200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf132 gene product has been provisionally designated C6orf132 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15218R-CY5

Anti-C6ORF132 Rabbit Polyclonal Antibody (Cy5)

Catalog Number: (BOSSBS-15218R-CY5)
Supplier: Bioss
Description: Making up nearly 6% of the human genome, chromosome 6 contains around 1200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf132 gene product has been provisionally designated C6orf132 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15251R-CY3

Anti-C6ORF62 Rabbit Polyclonal Antibody (Cy3)

Catalog Number: (BOSSBS-15251R-CY3)
Supplier: Bioss
Description: Making up nearly 6% of the human genome, chromosome 6 contains around 1200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf62 gene product has been provisionally designated C6orf62 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15255R-CY3

Anti-C6ORF97 Rabbit Polyclonal Antibody (Cy3)

Catalog Number: (BOSSBS-15255R-CY3)
Supplier: Bioss
Description: Making up nearly 6% of the human genome, chromosome 6 contains around 1200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf97 gene product has been provisionally designated C6orf97 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15216R-FITC

Anti-C6ORF129 Rabbit Polyclonal Antibody (FITC)

Catalog Number: (BOSSBS-15216R-FITC)
Supplier: Bioss
Description: C6orf129 is making up nearly 6% of the human genome, chromosome 6 contains around 1200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf129 gene product has been provisionally designated C6orf129 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15217R-FITC

Anti-C6ORF130 Rabbit Polyclonal Antibody (FITC)

Catalog Number: (BOSSBS-15217R-FITC)
Supplier: Bioss
Description: C6orf130 is making up nearly 6% of the human genome, chromosome 6 contains around 1200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf130 gene product has been provisionally designated C6orf130 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-15249R-HRP

Anti-C6ORF57 Rabbit Polyclonal Antibody (HRP)

Catalog Number: (BOSSBS-15249R-HRP)
Supplier: Bioss
Description: Making up nearly 6% of the human genome, chromosome 6 contains around 1200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf57 gene product has been provisionally designated C6orf57 pending further characterisation.
UOM: 1 * 100 µl
Image Unavailable-ABCAAB90739-100

Anti-Melanoma Associated Antigen 100+ / 25kDa Mouse Monoclonal Antibody [clone: NKI-C3]

Catalog Number: (ABCAAB90739-100)
Supplier: Abcam
Description: Mouse monoclonal [NKI-C3] to Melanoma Associated Antigen 100+ / 25kDa.
UOM: 1 * 100 µG
Image Unavailable-BOSSBS-9629R-A680

Anti-C16orf7 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (BOSSBS-9629R-A680)
Supplier: Bioss
Description: Chromosome 16 encodes over 900 genes in approximately 90 million base pairs, makes up nearly 3% of human cellular DNA and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterised by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumour growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.
UOM: 1 * 100 µl
Image Unavailable-USBIL9190-12L-100

Anti-Lysosome Associated Membrane Protein 2 Rat Monoclonal Antibody [clone: 10F753]

Catalog Number: (USBIL9190-12L-100)
Supplier: US Biological
Description: Anti-Lysosome Associated Membrane Protein 2 Rat Monoclonal Antibody [clone: 10F753]
UOM: 1 * 100 µG
Image Unavailable-USBIA0868-37B

Anti-Adeno-Associated Virus 2 Replicase Mouse Monoclonal Antibody [clone: 5F106]

Catalog Number: (USBIA0868-37B)
Supplier: US Biological
Description: Anti-Adeno-Associated Virus 2 Replicase Mouse Monoclonal Antibody [clone: 5F106]
UOM: 1 * 50 µG
Image Unavailable-USBIL9190-07J

Anti-Lysosome Associated Membrane Protein 1 Mouse Monoclonal Antibody (APC (Allophycocyanin)) [clone: 9A179]

Catalog Number: (USBIL9190-07J)
Supplier: US Biological
Description: Anti-Lysosome Associated Membrane Protein 1 Mouse Monoclonal Antibody (APC (Allophycocyanin)) [clone: 9A179]
UOM: 1 * 100 Tests
Image Unavailable-USBIL9190-13G

Anti-Lysosome Associated Membrane Protein 2 Rat Monoclonal Antibody (FITC (Fluorescein)) [clone: 5K54]

Catalog Number: (USBIL9190-13G)
Supplier: US Biological
Description: Anti-Lysosome Associated Membrane Protein 2 Rat Monoclonal Antibody (FITC (Fluorescein)) [clone: 5K54]
UOM: 1 * 500 µG
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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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The original product is no longer available. The replacement shown is available.
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