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(±)-2,2-Difluoro-1-methylcyclopropanecarboxylic+acid


144,674  results were found

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Supplier:  Matrix Scientific
Description:   2-{[3-(Trifluoromethyl)phenyl]amino}isonicotinic acid ≥97%
Supplier:  Bioss
Description:   C22orf43 (chromosome 22 open reading frame 43), also known as MGC33025 or MGC75009, is a 229 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.

Supplier:  Bioss
Description:   ANKRD54 is a 300 amino acid protein that contains four ankyrin repeats and is expressed as two alternatively spliced isoforms. The gene encoding human ANKRD54 maps to chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.
Supplier:  Rockland Immunochemical
Description:   Anti-Fructosyl-amino acid oxidase has been assayed against 1.0 µg of Fructosyl-Amino Acid Oxidase (E.coli) in a standard capture ELISA using ABTS (2,2’-azino-bis-[3-ethylbenthiazoline-6-sulfonic acid])
Supplier:  TCI America
Description:   CAS Number: 15042-01-0
MDL Number: MFCD00010552
Molecular Formula: C9H12O6
Molecular Weight: 216.19
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Melting point (°C): 210
Specific rotation [a]20/D: 10 deg (C=5, MeOH)
MSDS SDS
Supplier:  Bioss
Description:   CCDC117 is a 279 amino acid protein that is expressed as multiple alternatively spliced isoforms and is encoded by a gene which maps to human chromosome 22. Chromosome 22 houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia chromosome and the subsequent production of the novel fusion protein Bcr-Abl, a potent cell proliferation activator found in several types of leukemias.
Catalog Number: (80058-790)

Supplier:  MilliporeSigma
Description:   (Trp). White solid. Purity: >= 98% by titration. Soluble in H2O. RTECS YN6130000, CAS 73-22-3, M.W. 204.2. WARNING! May be carcinogenic/teratogenic.
MSDS SDS
Supplier:  THERMO FISHER SCIENTIFIC CHEMICALS
Description:   EDTA tripotassium salt dihydrate 99+%
Supplier:  TCI America
Description:   9,9-Didecylfluorene-2,7-diboronic Acid Bis(pinacol) Ester, Purity: >98.0%(HPLC), Cas no. 711026-06-1, Molecular formula: C45H72B2O4, Synonyms: 2,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9,9-didecylfluorene, Size: 1G
MSDS SDS
Supplier:  BeanTown Chemical
Description:   CAS: 1120-71-4; EC No: 214-317-9; MDL No: MFCD00005355; RTECS: RP5425000 UN No: UN2811; Haz Class: 6.1; Packing Group: III Solid; Molecular Formula: C3H6O3S; MW: 122.14 Melting Point: 30-33°; Boiling Point: 180°/30 mmHg; Flash point: 110°C (230°F) Density (g/mL): 1.392 Moisture Sensitive
MSDS SDS

Supplier:  Matrix Scientific
Description:   Matrix Scientific Part Number: 034874-500MG , MDL Number: MFCD03371464
Supplier:  Bioss
Description:   C22orf31, also known as HS747E2A or bK747E2.1, is a 290 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.

Supplier:  Matrix Scientific
Description:   Matrix Scientific Part Number: 041098-250MG , MDL Number: MFCD12028542
Supplier:  MilliporeSigma

Supplier:  Bioss
Description:   C22orf37 (chromosome 22 open reading frame 37), also known as FLJ40542, is a 170 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.
Catalog Number: (77102-720)

Supplier:  AMBEED, INC
Description:   6-(1H-pyrazol-1-yl)nicotinic acid 97%
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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 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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The original product is no longer available. The replacement shown is available.
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