2,3-Bis(amino((2-aminophenyl)thio)methylene)succinonitrile+compou
Supplier:
TCI America
Description:
CAS Number: 23628-31-1
MDL Number: MFCD00233711 Molecular Formula: C6H6N2O2 Molecular Weight: 138.13 Purity/Analysis Method: >98.0% (HPLC,T) Form: Crystal Melting point (°C): 315
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:
(76098-860)
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.
Catalog Number:
(TCD0504-25G)
Supplier:
TCI America
Description:
CAS Number: 67-43-6
MDL Number: MFCD00004289 Molecular Formula: C14H23N3O10 Molecular Weight: 393.35 Purity/Analysis Method: >98.0% (T) Form: Crystal Melting point (°C): 220
Catalog Number:
(76107-166)
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:
(77440-718)
Supplier:
Bioss
Description:
EAN57 is a 59 amino acid protein encoded by the C22orf33 protein. 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.
Supplier:
Honeywell Research Chemicals
Description:
Detritylation Solution contains 10% Dichloroacetic acid (DCA) in Toluene (v/v), suitable for use with DNA/RNA synthesis instruments. Packaged in 20-liter steel NOWPak containers that are returned for refill. Sold only under contract.
Catalog Number:
(101410-880)
Supplier:
Electron Microscopy Sciences
Description:
Aniline Blue Electron Microscopy Sciences solution is a prepared, ready-to-use, high quality staining solutions for standard staining procedures used by the Biological Staining Commission and the Armed Forces Institute of Pathology. Available in concentrations of 2.5% in 2% Acetic Acid, Phosphomolybdic Acid Solution, and with Orange G.
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Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
EDTA tetrasodium salt hydrate 98%, pure
Supplier:
AMBEED, INC
Description:
EDTA tetrasodium salt hydrate ≥98%
Supplier:
AMBEED, INC
Description:
(2S,3S)-2,3-Bis(pivaloyloxy)succinic acid, Purity: 98%, CAS Number: 76769-55-6, Appearance: Form: powder Colour: white, Storage: Sealed in dry, Room Temperature, Size: 25g
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:
(77686-538)
Supplier:
AMBEED, INC
Description:
6-Oxo-piperidine-2-carboxylic acid ≥95%
Supplier:
TCI America
Description:
CAS Number: 1670-82-2
MDL Number: MFCD00210441 Molecular Formula: C9H7NO2 Molecular Weight: 161.16 Purity/Analysis Method: >98.0% (HPLC,T) Form: Crystal Melting point (°C): 257
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 021136-1G , MDL Number: MFCD08275296
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.
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