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2-(4-Chloro-3-nitrobenzoyl)benzoic+acid
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2-(4-Chloro-3-nitrobenzoyl)benzoic+acid
Catalog Number:
(76194-876)
Supplier:
Prosci
Description:
CD6 is a type I transmembrane glycoprotein that contains a 24-amino acid signal sequence, three extracellular “scavenger receptor cysteine-rich” (SRCR) domains, a membrane-spanning domain and a 44-amino acid cytoplasmic domain. The CD6 glycoprotein is tyrosine phosphorylated during TCR-mediated T cell activation. CD6 shows significant homology to CD5. CD6 is present on mature thymocytes, peripheral T cells and a subset of B cells. antibody to CD6 can be used to deplete T cells from bone marrow transplants to prevent graft versus host disease.
Catalog Number:
(TCB1629-005G)
Supplier:
TCI America
Description:
CAS Number: 23680-31-1
MDL Number: MFCD00066063 Molecular Formula: C15H21NO5 Molecular Weight: 295.34 Purity/Analysis Method: >98.0% (HPLC,T) Form: Crystal Melting point (°C): 59 Specific rotation [a]20/D: 22 deg (C=2, EtOH)
Catalog Number:
(101817-744)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 024262-500MG , MDL Number: MFCD00020036
Supplier:
AMBEED, INC
Description:
(R)-(+)-α-Lipoic acid ≥95%
Supplier:
AOB CHEM USA
Description:
2-Methoxy-6-(methylthio)benzoic acid ≥97%
Catalog Number:
(TCD0504-25G)
Supplier:
TCI America
Description:
CAS Number: 67-43-6
MDL Number: MFCD00004289 Molecular Formula: C14H23N3O10 Molecular Weight: 393.35 Purity/Analysis Method: >98.0% (T) Form: Crystal Melting point (°C): 220
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:
(10477-078)
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:
(77440-718)
Supplier:
Bioss
Description:
EAN57 is a 59 amino acid protein encoded by the C22orf33 protein. 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:
(10666-566)
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:
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
Supplier:
Spectrum Chemicals
Description:
(Ethylenedinitrilo)tetraacetic Acid, Powder is generally abbreviated as EDTA, a colorless, water soluble, aminopolycarboxylic acid and solid. It's used for its chelating properties and as a ligand. It is used by many industries for application ranging from sequestering agent to chelation therapy. Ungraded products supplied by Spectrum are indicative of a grade suitable for general industrial use or research purposes and typically are not suitable for consumption.
Supplier:
ALADDIN SCIENTIFIC
Description:
Alizarin complexone ≥95%
Catalog Number:
(TCP0874-025G)
Supplier:
TCI America
Description:
[Good's buffer component for biological research]
CAS Number: 76836-02-7 MDL Number: MFCD00064349 Molecular Formula: C8H18N2O6S2 Molecular Weight: 346.32 Purity/Analysis Method: >98.0% (T) Form: Crystal Color: White
Catalog Number:
(10666-568)
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:
Bachem Americas
Description:
Sequence: Boc-Arg(Pbf)-OH
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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
is still displayed and you need assistance, please call us at 1-800-932-5000.
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