231 Results for: "1,14-tetradecanediol acid"
Corrected to: 1,14-tetradecanedioic acid
jetPRIME®, DNA and siRNA Transfection Reagent, Polyplus-transfection
Supplier: Polyplus Transfection
jetPRIME® DNA and/or siRNA transfection reagent is a powerful, and versatile reagent designed to ensure high DNA transfection efficiency and excellent gene silencing in a variety of adherent cells.
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FreeZone® Freeze Dryer Accessories, Labconco®
Supplier: Labconco
Racks and supports hold test tubes, flasks and microwell plates for pre-freezing and freeze drying samples; clear canister holds chemical traps.
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Human Recombinant GDF-3 (from E. coli)
Supplier: Peprotech
Animal-Free Human GDF-3, Recombinat, Purity: Greater than 98% by SDS-PAGE gel and HPLC analyses, Host: E.coli, member of the TGF-beta superfamily of growth and differentiation factors, and is highly homologous to GDF-9, Synonyms: UNQ2222/PRO248, Size: 50UG
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![313376_260x190.jpg](https://occapi.avantorsciences.com/medias/313376-260x190.jpg?context=bWFzdGVyfGltYWdlc3w5NDQ1fGltYWdlL2pwZWd8YURReUwyZzFZUzg1TnpBMk1ETTBOekkwT0RrMEx6TXhNek0zTmw4eU5qQjRNVGt3TG1wd1p3fGY0MjhiMmY1ZGJjNTY3NDdlZDk5ZjMwMGEyYTdmYjNkY2IyNWE2ZmI1MTg2YTM4MjE0MTY4MmNiYjVmNTViMTE)
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Human XCL1 - Lymphotactin ELISA Kit, Rockland Immunochemicals
Supplier: Rockland Immunochemical
Human XCL1 - Lymphotactin AccuSignal ELISA Kit
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Mouse XCL1 - Lymphotactin ELISA Kit, Rockland Immunochemicals
Supplier: Rockland Immunochemical
Mouse XCL1 - Lymphotactin AccuSignal ELISA Kit
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Rat BMP-2 ELISA Kit, Rockland Immunochemicals
Supplier: Rockland Immunochemical
Rat BMP-2 AccuSignal ELISA Kit
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Mouse BMP-2 ELISA Kit, Rockland Immunochemicals
Supplier: Rockland Immunochemical
Mouse BMP-2 AccuSignal ELISA Kit
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Anti-C9ORF114 Rabbit Polyclonal Antibody (Cy5®)
Supplier: Bioss
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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Anti-C9ORF114 Rabbit Polyclonal Antibody (Cy3®)
Supplier: Bioss
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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Anti-C9ORF114 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))
Supplier: Bioss
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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Human IL-15 ELISA Kit, Rockland Immunochemicals
Supplier: Rockland Immunochemical
Human Interleukin-15 AccuSignal ELISA Kit
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Anti-C9ORF114 Rabbit Polyclonal Antibody (Alexa Fluor® 488)
Supplier: Bioss
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.
Expand 1 Items
Anti-C9ORF114 Rabbit Polyclonal Antibody (Alexa Fluor® 555)
Supplier: Bioss
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.
Expand 1 Items
Anti-C9ORF114 Rabbit Polyclonal Antibody (Alexa Fluor® 350)
Supplier: Bioss
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.
Expand 1 Items
Anti-C9ORF114 Rabbit Polyclonal Antibody (Cy7®)
Supplier: Bioss
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.
Expand 1 Items
Anti-C9ORF114 Rabbit Polyclonal Antibody (Alexa Fluor® 647)
Supplier: Bioss
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.
Expand 1 Items
Anti-C9ORF114 Rabbit Polyclonal Antibody (Cy5.5®)
Supplier: Bioss
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.
Expand 1 Items
Anti-C9ORF114 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))
Supplier: Bioss
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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Human BMP-2 ELISA Kit, Rockland Immunochemicals
Supplier: Rockland Immunochemical
Human BMP-2 AccuSignal ELISA Kit
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Anti-LNC1 Mouse Monoclonal Antibody [clone: LNC 1; LNC1;LNC-1]
Supplier: Biosensis
Tyrosine hydroxylase is an excellent marker for dopaminergic and noradrenergic neurons. Tyrosine hydroxylase (a.k.a. tyrosine 3-monooxygenase) is the enzyme responsible for catalyzing the conversion of the amino acid L-tyrosine to L-3,4-dihydroxyphenylalanine (L-DOPA). L-DOPA is a precursor for dopamine, which, in turn, is a precursor for the important neurotransmitters norepinephrine (noradrenaline) and epinephrine (adrenaline). Tyrosine hydroxylase catalyzes the rate limiting step in this synthesis of catecholamines. In humans, tyrosine hydroxylase is encoded by the TH gene, and the enzyme is present in the central nervous system (CNS), peripheral symphatic neurons and the adrenal medulla. The enzymatic activity of TH requires ferrous ions as cofactors and is believed to be regulated by phosphorylation. At least four isoforms of human TH have been identified which result from alternative splicing. Tyrosine hydroxylase, phenylalanine hydroxylase and tryptophan hydroxylase together make up the family of aromatic amino acid hydroxylases (AAAHs). http://en.wikipedia.org/wiki/Tyrosine_hydroxylase
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L-Series Positive Pressure Headgear, 3M™
Supplier: 3M
Comfortable respirators are safe and cost-effective. No fit testing required. Positive pressure airflow has no breathing resistance and helps provide a higher level of respiratory protection. Wide-view lens provides better downward and peripheral vision. The lightweight headgear can be worn with facial hair, prescription eyewear, or safety glasses.