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Description: 2,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9,9-dimethylfluorene, Purity: >98%, CAS: 325129-69-9, MF: C27H36B2O4, MW: 446.20, Synonyms: 9,9-Dimethylfluorene-2,7-diboronic Acid Bis(pinacol) Ester, Size: 1G
Catalog Number: 76219-510
Supplier: TCI America


Description: CAS Number: 79-43-6
MDL Number: MFCD00004223
Molecular Formula: C2H2Cl2O2
Molecular Weight: 128.94
Purity/Analysis Method: >98.0% (GC,T)
Form: Clear Liquid
Boiling point (°C): 193
Flash Point (°C): 170
Freezing point (°C): 13
Specific Gravity (20/20): 1.57
Catalog Number: TCD0308-500G
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: 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: Alizarin red S (sodium salt)
Catalog Number: 97062-616
Supplier: VWR

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: 76107-164
Supplier: Bioss


Description: BAPTA tetramethyl ester, Purity: 99%, CAS number: 125367-34-2, Molecular Formula: C26H32N2O10, synonym: 1,2-Bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid tetramethyl ester, Size: 5g
Catalog Number: AAH66907-MD
Supplier: Thermo Scientific Chemicals

Description: Membrane-permeable version of FLUO 3
Catalog Number: CA80051-690
Supplier: MilliporeSigma

Description: LAG-1 is CC chemokine that signals through the CCR5 receptor. LAG-1 is identical to MIP-1beta (ACT II isotype) except for two amino acid substitutions; arginine for histidine at position 22 and serine for glycine at position 47 of the mature protein. LAG-1 chemoattracts monocytes, and exhibits activity as an HIV suppressive factor. Recombinant human LAG-1 is a 7.7 kDa protein containing 69 amino acid residues.
Catalog Number: 10072-570
Supplier: Prosci


Description: For Synthesis
Catalog Number: CA8.00140.0250
Supplier: MilliporeSigma


Description: Grade Acs,Reagent Ph Eur, Cas Number 5808-22-0
Catalog Number: CA1.02498.0025
Supplier: MilliporeSigma

Description: Heptafluorobutyric acid 99%
Catalog Number: CAAAA14907-22
Supplier: Thermo Scientific Chemicals

Description: Thermo Scientific Pierce Ellman's Reagent (DTNB) reacts with sulfhydryl groups to yield a colored product, providing a reliable method to measure reduced cysteines and other free sulfhydryls in solution.
Catalog Number: CAPI22582
Supplier: Thermo Scientific

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: 76098-858
Supplier: Bioss


Description: CAS Number: 94-44-0
MDL Number: MFCD00023584
Molecular Formula: C13H11NO2
Molecular Weight: 213.24
Purity/Analysis Method: >98.0% (GC)
Form: Crystal
Boiling point (°C): 189
Flash Point (°C): 113
Freezing point (°C): 22
Catalog Number: TCN0083-025G
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: 10476-324
Supplier: Bioss


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