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3-(4-Thiazolyl)-L-alanine
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3-(4-Thiazolyl)-L-alanine
Catalog Number:
(89304-436)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to MARCKS (Phospho Ser162)
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.
Catalog Number:
(100278-860)
Supplier:
Indofine Chemical Company
Description:
Rare Organics & BioChemicals 1gm H-D-Ala-NH2. HCI 124.6 Room temperature.
Catalog Number:
(101851-838)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 041453-1G , MDL Number: MFCD01632072
Supplier:
Thermo Scientific Chemicals
Description:
1g CAS: 76387-70-7, MDL: MFCD01632072
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
Catalog Number:
(10264-164)
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.
Catalog Number:
(10264-166)
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
Catalog Number:
(80512-674)
Supplier:
MilliporeSigma
Description:
TAPI-0, CAS 143457-40-3, is a hydroxamate-based inhibitor of collagenase, gelatinase, and TACE (TNF-α converting enzyme/ADAM17; IC₅₀ = 100 nM).
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:
BeanTown Chemical
Description:
CAS: 122235-70-5; MDL No: MFCD00235897
Powder; Molecular Formula: C23H26N2O6; MW: 426.46
Catalog Number:
(10264-160)
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.
Catalog Number:
(100278-636)
Supplier:
Indofine Chemical Company
Description:
Rare Organics & BioChemicals 1gm H-Ala(3-Cl)-OMe.HCI 174.00 Room temperature.
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
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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.
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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