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2,2-Difluorocyclopropanecarboxylic+acid
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2,2-Difluorocyclopropanecarboxylic+acid
Supplier:
Adipogen
Description:
For the labeling of amino acids and their detection in picomolar amounts.
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.
Catalog Number:
(102837-594)
Supplier:
Matrix Scientific
Description:
4-(4-Methylphenyl)-1H-pyrrole-3-carboxylic acid ≥97%
Catalog Number:
(76109-876)
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.
Catalog Number:
(101824-916)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 027820-500MG , MDL Number: MFCD01993642
Catalog Number:
(103616-152)
Supplier:
Sino Biological
Description:
A DNA sequence encoding human IL22(NP_065386.1) (Ala34-Ile179) was expressed with a N-terminal Met.
Catalog Number:
(76108-240)
Supplier:
Bioss
Description:
Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. 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. CCDC134 (coiled-coil domain containing 134), also known as MGC21013 or FLJ22349, is a 229 amino acid protein encoded by a gene mapping to human chromosome 22.
Catalog Number:
(101824-362)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 027532-500MG , MDL Number: MFCD08681035
Supplier:
APOLLO SCIENTIFIC
Description:
Glyoxylic acid monohydrate 97%
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
L(-)-Tryptophan 99%
Catalog Number:
(RL200-603-236S)
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])
Catalog Number:
(76483-462)
Supplier:
AAT BIOQUEST INC
Description:
Calcein, also known as fluorexon, fluorescein complex, is a fluorescent calcium indicator with an excitation and emission wavelengths of 495 and 515 nm respectively.
Catalog Number:
(10666-576)
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.
Catalog Number:
(10311-190)
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:
BeanTown Chemical
Description:
CAS: 6192-52-5; EC No: 203-180-0; MDL No: MFCD00142137; RTECS: XT6300000
UN No: UN2585; Haz Class: 8; Packing Group: III
Crystalline; Linear Formula: CH3C6H4SO3H·H2O; Molecular Formula: C7H8O3S·H2O; MW: 190.22
Melting Point: 103-106°; Boiling Point: 140°/22 mmHg; Flash point: 150°C (302°F)
Density (g/mL): 1.24
Hygroscopic
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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
is still displayed and you need assistance, please call us at 1-800-932-5000.
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