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Catalog Number: (89320-386)
Supplier: Genetex
Description: Rabbit Polyclonal antibody to IL22 (interleukin 22)


Catalog Number: (TCD2286-025G)
Supplier: TCI America
Description: CAS Number: 40278-59-9
MDL Number: MFCD00191424
Molecular Formula: C23H28O4
Molecular Weight: 368.47
Purity/Analysis Method: >98.0% (HPLC)
Form: Crystal
Melting point (°C): 210

Catalog Number: (76549-460)
Supplier: Mortech Manufacturing
Description: No. 22 Blades for all post-mortem dissection procedures. Buy in bulk for convenience and savings.


Catalog Number: (TCF0112-025G)
Supplier: TCI America
Description: CAS Number: 456-22-4
MDL Number: MFCD00002530
Molecular Formula: C7H5FO2
Molecular Weight: 140.11
Purity/Analysis Method: >98.0% (GC,T)
Form: Crystal
Melting point (°C): 186

Supplier: Peprotech
Description: Produced from sera of rabbits immunized with highly pure Recombinant Human IL-22. Anti­Human IL-22­specific antibody was purified by affinity chromatography and then biotinylated.

Catalog Number: (77440-764)
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.


Supplier: Thermo Scientific Chemicals
Description: Fieser: 8,313 10,252 13,172
Supplier: TCI America
Description: CAS Number: 719-22-2
MDL Number: MFCD00001601
Molecular Formula: C14H20O2
Molecular Weight: 220.31
Purity/Analysis Method: >98.0% (GC)
Form: Crystal
Melting point (°C): 67
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.


Supplier: TCI America
Description: CAS Number: 180186-94-1
MDL Number: MFCD06797115
Molecular Formula: C21H18N2O2
Molecular Weight: 330.39
Purity/Analysis Method: >98.0% (HPLC,N)
Form: Crystal
Melting point (°C): 225
Specific rotation [a]20/D: 360 deg (C=1, CH2Cl2)
Catalog Number: (10666-572)
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.


Supplier: VWR International
Description: VWR® Graduated Addition/Dropping funnels with PTFE Stopcocks are made from Borosilicate 3.3 glass, ASTM 438, Type 1, Class A standard.

UL Listed

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: (10664-270)
Supplier: Bioss
Description: Neuronal axonal membrane protein Nap-22, also designated neuronal tissue-enriched acidic protein or brain acid soluble protein (BASP1), is a Ca2+-dependent calmodulin-binding protein that is important for neuronal sprouting and plasticity. Nap-22 is abundant in brain nerve terminals and is also present in significant amounts in kidney, testis and lymphoid tissue. Nap-22 undergoes N-terminal myristoylation for membrane localization. It has been characterized as a major protein of neuronal rafts, which are known to preferentially bind membranes containing cholesterol. Nap-22 is a crucial protein active in neurite outgrowth and synaptic plasticity.


Catalog Number: (10666-554)
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.


Supplier: TCI America
Description: CAS Number: 218301-22-5
MDL Number: MFCD01863558
Molecular Formula: C8H4FNO
Molecular Weight: 149.12
Purity/Analysis Method: >98.0% (GC)
Form: Crystal
Melting point (°C): 85

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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 call is still displayed and you need assistance, please call us at 1-800-932-5000.
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