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3,5-Bis(trifluoromethyl)benzamidoxime


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Catalog Number: (AAAL02833-03)

Supplier:  Thermo Scientific Chemicals
Description:   H-DL-Phe(4-Br)-OH. Grade: 98+, Melting Point ca 262*[degree]C. Boiling Point C: NA. C9H10BrNO2. 14091-15-7.
MSDS SDS
Supplier:  MilliporeSigma
MSDS SDS
Supplier:  Thermo Scientific Chemicals
Description:   1g CAS: 76387-70-7, MDL: MFCD01632072
MSDS SDS
Supplier:  Thermo Scientific Chemicals
Description:   H-DL-Phe(2-F)-OH. Grade:98, Melting Point C243-246*. Boiling Point C:NA. C9H10FNO2. 2629-55-2. HARMFUL
MSDS SDS

Supplier:  Bioss
Description:   CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Supplier:  Bioss
Description:   CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Supplier:  Matrix Scientific
Description:   Matrix Scientific Part Number: 041542-1G , MDL Number: MFCD00672562
Supplier:  BeanTown Chemical
Description:   CAS: 122235-70-5; MDL No: MFCD00235897 Powder; Molecular Formula: C23H26N2O6; MW: 426.46
MSDS SDS
Supplier:  Indofine Chemical Company
Description:   Rare Organics & BioChemicals 1gm H-Ala(3-Cl)-OMe.HCI 174.00 Room temperature.
Small Business Enterprise Minority or Woman-Owned Business Enterprise
Catalog Number: (75788-746)

Supplier:  Prosci
Description:   Recombinant Human Interleukin-2 is a highly purified protein with a molecular weight of approximately 15,300 Daltons. The chemical name is des-alanyl-1, serine-125 Human Interleukin-2. It is produced by recombinant DNA technology using a genetically engineered E. coli strain containing an analog of the human interleukin-2 gene. Genetic engineering techniques were used to modify the Human IL-2 gene, and the resulting expression clone encodes a modified Human IL-2. This recombinant form differs from native Interleukin-2 in following ways: 1) it is not glycosylated; 2) the molecule has no N-terminal alanine; 3) the molecule has serine substituted for cysteine at amino acid position 125; 4) the aggregation state of molecule is likely to be different from that of native IL-2.

Supplier:  Matrix Scientific
Description:   Matrix Scientific Part Number: 041453-1G , MDL Number: MFCD01632072
Supplier:  AMBEED, INC
Description:   3-((2-(Pyridin-2-yl)-6-(1,2,4,5-tetrahydro-3H-benzo[d]azepin-3-yl)pyrimidin-4-yl)amino)propanoic acid, Purity: 98%, CAS Number: 1373422-53-7, Appearance: White to off-white powder or crystals, Storage: Keep in dark place, Inert atmosphere, 2-8 C, Size: 10mg

Supplier:  Bioss
Description:   CSAD is a 493 amino acid protein that exists as a homodimer and belongs to the group II decarboxylase family. CSAD catalyzes the conversion of 3-sulfino-L-alanine to hypotaurine and carbon dioxide, binds pyridoxal phosphate as a cofactor and undergoes alternative splicing to produce three isoforms. The gene encoding CSAD maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.

Supplier:  Bioss
Description:   DR1, also known as NC2∫ (negative cofactor 2 subunit ∫), is a TFIID (TATA box-binding protein)-associated protein. DR1 localizes to the nucleus and contains an N-terminal histone fold motif, a TFIID-binding domain and an alanine and glutamine rich region. Via its histone fold motif, DR1 forms a heterodimer with NC2Ã¥ (DRAP1) to comprise the conserved eukaryotic complex, NC2 (negative cofactor 2). The NC2 complex can both positively and negatively regulate transcription by RNA Pol II. More specifically, NC2 acts as a repressor of TATA-dependent transcription and acts as an activator for DPE-dependent transcription. NC2 represses RNA Pol II transcription by binding to TFIID and inhibiting association of the transcription factors TFIIA and TFIIB. NC2 activity is regulated by phosphorylation. Both subunits, NC2Ã¥ and DR1, are phosphorylated in vivo.

Supplier:  Bioss
Description:   GPCR TGR7.
Supplier:  Thermo Scientific Chemicals
Description:   H-DL-Phe(4-F)-OH. Grade:98+, Melting Point ca 254*[degree]C. Boiling Point C:NA. C9H10FNO2. 51-65-0. HARMFUL
MSDS SDS
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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.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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