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Catalog Number: (77518-350)
Supplier: AFG Bioscience
Description: Human PMP22 (Peripheral Myelin Protein 22) ELISA Kit


Catalog Number: (10343-094)
Supplier: Bioss
Description: Cytokine that contributes to the inflammatory response in vivo.


Catalog Number: (10343-086)
Supplier: Bioss
Description: Cytokine that contributes to the inflammatory response in vivo.


Supplier: Thermo Scientific Chemicals
Description: Nitrilotriacetic acid 99%
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: (TCH0181-005G)
Supplier: TCI America
Description: CAS Number: 16289-95-5
MDL Number: MFCD00003781
Molecular Formula: C18H10O6
Molecular Weight: 322.27
Purity/Analysis Method: >98.0% (T)
Form: Crystal

Catalog Number: (89280-496)
Supplier: Genetex
Description: Mouse monoclonal antibody [LOX19-22] to LOX-1 (soluble)


Supplier: Abcam
Description: Rabbit monoclonal [EPR19944-246] to IL-22 - BSA and Azide free (Capture).

New Product

Supplier: TCI America
Description: CAS Number: 918-22-9
MDL Number: MFCD00153110
Molecular Formula: C6Br2F12
Molecular Weight: 459.85
Purity/Analysis Method: >98.0% (GC)
Form: Clear Liquid
Boiling point (°C): 150
Specific Gravity (20/20): 2.10
Storage Temperature: 0-10°C

SDS

Catalog Number: (TCT1166-010G)
Supplier: TCI America
Description: CAS Number: 480-22-8
MDL Number: MFCD00001250
Molecular Formula: C14H10O3
Molecular Weight: 226.23
Purity/Analysis Method: >95.0% (HPLC,T)
Form: Crystal
Color: Pale Yellow
Melting point (°C): 181

Catalog Number: (TCP1142-025ML)
Supplier: TCI America
Description: CAS Number: 25564-22-1
MDL Number: MFCD00036631
Molecular Formula: C10H16O
Molecular Weight: 152.24
Purity/Analysis Method: >95.0% (GC)
Form: Clear Liquid
Color: Colorless
Boiling point (°C): 115
Flash Point (°C): 110
Specific Gravity (20/20): 0.92

SDS


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.


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: (10476-324)
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.


Catalog Number: (77516-650)
Supplier: AFG Bioscience
Description: Human ADAM22 (A Disintegrin And Metalloprotease 22) ELISA Kit


Supplier: TCI America
Description: CAS Number: 35144-22-0
MDL Number: MFCD03788286
Molecular Formula: C7H10N2O2S
Molecular Weight: 186.23
Purity/Analysis Method: >98.0% (GC)
Form: Crystal
Melting point (°C): 82

SDS

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