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(±)-2,2-Difluoro-1-methylcyclopropanecarboxylic+acid
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(±)-2,2-Difluoro-1-methylcyclopropanecarboxylic+acid
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
Solid; 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
Catalog Number:
(TCB1629-005G)
Supplier:
TCI America
Description:
CAS Number: 23680-31-1
MDL Number: MFCD00066063 Molecular Formula: C15H21NO5 Molecular Weight: 295.34 Purity/Analysis Method: >98.0% (HPLC,T) Form: Crystal Melting point (°C): 59 Specific rotation [a]20/D: 22 deg (C=2, EtOH)
Catalog Number:
(89512-492)
Supplier:
Abgent
Description:
Polyclonal antibody, Isotype: Rabbit Ig species reactivity: human , Gene ID: 11651, Target/Specificity: generated from rabbits immunized with a KLH conjugated synthetic peptide between 22-49 amino acids from the N-terminal region of mouse Akt1
Catalog Number:
(76483-132)
Supplier:
AAT BIOQUEST INC
Description:
Calcium measurement is critical for numerous biological investigations.
Supplier:
ALADDIN SCIENTIFIC
Description:
4-Amino-3-(trifluoromethoxy)benzoic acid ≥98%
Catalog Number:
(10477-072)
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:
(10477-082)
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:
(102894-604)
Catalog Number:
(10477-074)
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:
(10257-762)
Supplier:
Bioss
Description:
TNRC6B is a 1,723 amino acid protein that exists as two alternatively spliced isoforms and is thought to be involved in mRNA cleavage events. Expressed ubiquitously, TNRC6B contains one glycine/tryptophan (GW)-rich N-terminal domain, one central glutamine-rich region and one C-terminal RNA recognition motif and is encoded by a gene that maps to human chromosome 22. 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:
Matrix Scientific
Description:
MF=C23H44N2O6 MW=444.62 CAS=560088-79-1 MDL=MFCD06796877 5G
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Heptafluorobutyric acid 99%
Supplier:
AMBEED, INC
Description:
[6,6]-Phenyl-C61-butyric acid methyl ester 99.5%
Supplier:
MP Biomedicals
Description:
Calcein is used as an Indicator for the determination of calcium by titration with EDTA. Suitable for fluorometric determination of calcium.
Catalog Number:
(10476-330)
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.
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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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