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1,6-Dichlorohexane
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1,6-Dichlorohexane
Supplier:
Electron Microscopy Sciences
Description:
NE45 eyepiece scale is surface chrome picture, 10 mm diameter separated in degrees, 16 mm full protractor scale.
Catalog Number:
(77980-415)
Supplier:
LGC STANDARDS
Description:
Cladinose, TRC, LGC Standards
Catalog Number:
(10278-420)
Supplier:
Bioss
Description:
ZNF843 is a 348 amino acid protein that is encoded by a gene which maps to chromosome 16. 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 characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16 through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor 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. The ZNF843 gene product has been provisionally designated MGC46336 pending further characterization.
Catalog Number:
(RK22998)
Supplier:
Restek
Description:
Includes twelve hex keys (Allen wrenches): 0.050", <sup>1</sup>/<sub>16</sub>", <sup>5</sup>/<sub>64</sub>", <sup>3</sup>/<sub>32</sub>", <sup>7</sup>/<sub>64</sub>", <sup>1</sup>/<sub>8</sub>", <sup>9</sup>/<sub>64</sub>", <sup>5</sup>/<sub>32</sub>", <sup>3</sup>/<sub>16</sub>", <sup>7</sup>/<sub>32</sub>", <sup>1</sup>/<sub>4</sub>", and <sup>5</sup>/<sub>16</sub>".
Catalog Number:
(10667-044)
Supplier:
Bioss
Description:
ANKS3 is a 656 amino acid protein that contain six ANK repeats and one SAM (sterile alpha motif) domain. The gene encoding ANKS3 maps to human chromosome 16. Chromosome 16, which is associated with a variety of genetic disorders, encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
Catalog Number:
(102530-916)
Supplier:
Matrix Scientific
Description:
MF=C5H9BRO MW=165.04 CAS=25637-16-5 MDL=MFCD07371501 5G
Supplier:
Matrix Scientific
Description:
MF=C6H12O MW=100.16 CAS=2987-16-8 MDL=MFCD00042807 25G
Supplier:
Matrix Scientific
Description:
MF=C5H6BRN3 MW=188.03 CAS=1209458-16-1 MDL=MFCD13193672 5G
Supplier:
United Scientific Supplies
Description:
Solid, black stoppers contain a high percentage of pure rubber and weigh less than neoprene.
Supplier:
AMBEED, INC
Description:
Milrinone 98%
Catalog Number:
(10249-496)
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 characterized 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 tumor 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. The KIAA1576 gene product has been provisionally designated KIAA1576 pending further characterization.
Catalog Number:
(10278-424)
Supplier:
Bioss
Description:
ZNF843 is a 348 amino acid protein that is encoded by a gene which maps to chromosome 16. 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 characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16 through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor 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. The ZNF843 gene product has been provisionally designated MGC46336 pending further characterization.
Supplier:
Thermo Scientific Chemicals
Description:
Locostatin is a cell permeable, potent inhibitor of Raf kinase inhibitor protein (RKIP)/Raf1 kinase interaction and an inhibitor of cell migration
Supplier:
Matrix Scientific
Description:
MF=C6H7No2 MW=125.13 Cas=4664-16-8 1G
Catalog Number:
(10062-656)
Supplier:
Prosci
Description:
16 amino acid peptide near the carboxy terminus of human RRAS2.
Catalog Number:
(10278-406)
Supplier:
Bioss
Description:
ZNF843 is a 348 amino acid protein that is encoded by a gene which maps to chromosome 16. 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 characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16 through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor 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. The ZNF843 gene product has been provisionally designated MGC46336 pending further characterization.
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 is still displayed and you need assistance, please call us at 1-800-932-5000.
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
is still displayed and you need assistance, please call us at 1-800-932-5000.
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 Regulatory_Affairs@vwr.com
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