4-Chloro-2,3-difluorobenzonitrile
Catalog Number:
(TCE0095-025G)
Supplier:
TCI America
Description:
CAS Number: 15375-84-5
MDL Number: MFCD00054451 Molecular Formula: C10H16N2O8 Molecular Weight: 389.13 Purity/Analysis Method: >95.0% (T) Form: Crystal
Catalog Number:
(76772-896)
Supplier:
AMBEED, INC
Description:
4-Chloro-2-fluoro-5-sulfamoylbenzoic acid 98%
Catalog Number:
(10477-078)
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:
(TCP0874-025G)
Supplier:
TCI America
Description:
[Good's buffer component for biological research]
CAS Number: 76836-02-7 MDL Number: MFCD00064349 Molecular Formula: C8H18N2O6S2 Molecular Weight: 346.32 Purity/Analysis Method: >98.0% (T) Form: Crystal Color: White
Supplier:
ALADDIN SCIENTIFIC
Description:
Alizarin complexone ≥95%
Catalog Number:
(77372-166)
Supplier:
AOB CHEM USA
Description:
2-Amino-5-pyrimidineboronic acid ≥97%
Supplier:
TCI America
Description:
2,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9,9-dimethylfluorene, Purity: >98%, CAS: 325129-69-9, MF: C27H36B2O4, MW: 446.20, Synonyms: 9,9-Dimethylfluorene-2,7-diboronic Acid Bis(pinacol) Ester, Size: 1G
Catalog Number:
(102830-626)
Supplier:
BioVendor
Description:
Recombinant protein contains amino acids no. 22–243 of the protein acc.no. P16562 in UniProtKB. Total 232 AA. MW: 26.32 kDa (calculated). N-Terminal His-tag (10 extra AA)
Supplier:
Matrix Scientific
Description:
MF=C30H26N2O13 MW=622.55 CAS=1461-15-0 MDL=MFCD00005049 100G
Catalog Number:
(101817-744)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 024262-500MG , MDL Number: MFCD00020036
Catalog Number:
(76121-134)
Supplier:
Bioss
Description:
C22orf9 is a 404 amino acid protein that exists as three alternatively spliced isoforms and is 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, chromosome 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:
(76098-812)
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:
(76098-810)
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.
Supplier:
AOB CHEM USA
Description:
4-(1,3,4-oxadiazol-2-ylphenyl)boronic acid ≥97%
Catalog Number:
(10476-322)
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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