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


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: TCD2286-025G
Supplier: TCI America

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


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
Catalog Number: TCF0112-025G
Supplier: TCI America

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: 10771-494
Supplier: Peprotech


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.
Catalog Number: 77440-764
Supplier: Bioss


Description: Fieser: 8,313 10,252 13,172
Catalog Number: CAAAA15603-14
Supplier: Thermo Scientific Chemicals

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: TCD2256-005G
Supplier: TCI America

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.
Catalog Number: 76108-240
Supplier: Bioss


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: TCM1401-500MG
Supplier: TCI America

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.
Catalog Number: 10666-572
Supplier: Bioss


Description: VWR® Graduated Addition/Dropping funnels with PTFE Stopcocks are made from Borosilicate 3.3 glass, ASTM 438, Type 1, Class A standard.
Catalog Number: 75997-994
Supplier: VWR International

UL Listed


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: 76121-134
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: 10664-270
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.
Catalog Number: 10666-554
Supplier: Bioss


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
Catalog Number: TCC2692-5G
Supplier: TCI America

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