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chromatography+columns+HyClone+products+(Cytiva)
Supplier:
AGILENT TECHNOLOGIES, INC (CSD) CA
Description:
Agilent nebulizers and supplies are equivalent to PerkinElmer AA nebulizer components.
Supplier:
AGILENT TECHNOLOGIES, INC (CSD) CA
Description:
High-quality supplies for special function valves such as 2D-LC valves.
Catalog Number:
(89297-122)
Supplier:
Genetex
Description:
Goat polyclonal antibody to PTF1A / PFT1-P48
Supplier:
GE Healthcare - Life Sciences
Description:
Polycap HD (Heavy Duty) capsule filter offers a broad range of particle size retention ratings and excellent filtrate purity with polypropylene filters (PP).
Supplier:
AGILENT TECHNOLOGIES, INC (CSD) CA
Description:
Typical supplies for VGA 77 Vapor Generation Accessory used with Agilent flame AA Spectrometers.
Supplier:
AGILENT TECHNOLOGIES, INC (CSD) CA
Description:
Agilent supplies a range of cleaning and maintenance supplies for your LC/MS.
Catalog Number:
(89273-896)
Supplier:
Genetex
Description:
Mouse monoclonal antibody [2A9] to ERCC1
Catalog Number:
(89296-270)
Supplier:
Genetex
Description:
Goat polyclonal antibody to P2RX7 / P2X7 receptor
Catalog Number:
(89304-048)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to MEK-2 (Phospho Thr394)
Catalog Number:
(89289-338)
Supplier:
Genetex
Description:
Rabbit polyclonal antibody to PAK3 (phospho Ser154)
Catalog Number:
(89304-436)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to MARCKS (Phospho Ser162)
Catalog Number:
(89304-510)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to SHP-2 (Phospho Tyr542)
Catalog Number:
(89304-590)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to GSK3 alpha
Catalog Number:
(10494-856)
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 FAM96B gene product has been provisionally designated FAM96B pending further characterization.
Catalog Number:
(10490-428)
Supplier:
Bioss
Description:
C9orf150 is a 231 amino acid protein encoded by a gene that maps to human chromosome 9p23. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Catalog Number:
(10490-396)
Supplier:
Bioss
Description:
C9orf114 is a 376 amino acid protein encoded by a gene that maps to human chromosome 9q34.11. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
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