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2,2\'-Dithiodi(benzoic+acid)
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2,2\'-Dithiodi(benzoic+acid)
Catalog Number:
(10750-892)
Supplier:
Prosci
Description:
TMEM184B Antibody: TMEM184B, also known as C22orf5, is a 407 amino acid multi-pass membrane protein and represents a novel gene in the activation of the MAPK signaling pathway. The gene encoding TMEM184B maps to human chromosome 22; mutations in several of the genes in chromosome 22 are involved in the development of autism, schizophrenia, Phelan-McDermid syndrome and Neurofibromatosis type 2, suggesting that TMEM184B may play a role in these syndromes.
Supplier:
BeanTown Chemical
Description:
CAS: 65094-22-6; MDL No: MFCD00069118
Liquid; Molecular Formula: C5H10BrF2O3P; MW: 267.01
Boiling Point: 40-41°/0.05 mmHg; Flash point: <gt/>110°C (<gt/>230°F)
Density (g/mL): 1.503; Refractive Index: 1.417
Supplier:
Matrix Scientific
Description:
Dimethyl-7,7'-dimethoxy[4,4'-bibenzo[d][1,3]dioxole]5,5'-dicarboxylate ≥95%
Supplier:
AMBEED, INC
Description:
(6-Bromo-2-methylpyridin-3-yl)boronic acid 98%
Catalog Number:
(103512-746)
Supplier:
Acros Organics
Description:
Sodium pivalate hydrate, Purity: 99%, CAS Number: 143174-36-1, Molecular weight: 142.13, Molecular formula: C5 H9 O2. Na. H2 O, Color: White to off-white, Form: Crystalline powder, Synonyms: Sodium trimethylacetate hydrate, Size: 10g
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 026120-25G , MDL Number: MFCD00191400
Catalog Number:
(76121-130)
Supplier:
Bioss
Description:
C22orf36 is a 315 amino acid protein that contains two LRR (leucine-rich) repeats and exists as two alternatively spliced isoforms. C22orf36 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:
(10311-196)
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: 37784-17-1; MDL No: MFCD00063226
Powder; Molecular Formula: C10H17NO4; MW: 215.25
Melting Point: 134-137°
Optical Rotation: [α]22/D +60°, c = 2 in acetic acid
Catalog Number:
(102837-048)
Supplier:
Matrix Scientific
Description:
2-{[3-(Trifluoromethyl)phenyl]amino}isonicotinic acid ≥97%
Supplier:
Thermo Scientific Chemicals
Description:
96+%,UN2586,Liquid,DANGER: CORROSIVE, irritates skin & eyes,1kg,3x1kg,CORROSIVE,
Supplier:
SPEX CERTIPREP LLC
Description:
Assurance® mixed multi-element quality control standards for AA & ICP.
Catalog Number:
(10477-060)
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:
(101823-664)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 027178-500MG , MDL Number: MFCD01825281
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 is still displayed and you need assistance, please call us at 1-800-932-5000.
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.
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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