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Supplier: Ambeed
Description: Sulfino-L-alanine hydrate, Purity: 98%, CAS Number: 207121-48-0, Appearance: Solid, Storage: Keep in dark place, Inert atmosphere, Store in freezer, under -20 deg C, Size: 1mg

Catalog Number: (10264-168)
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: (10264-162)
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: (10264-148)
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: (10264-160)
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: (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.


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.


Supplier: Ambeed
Description: 3-Cyclohexyl-D-alanine hydrate 98+%

Supplier: Matrix Scientific
Description: N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-alanine hydrate

Supplier: Ambeed
Description: (S)-2-Amino-3-cyclohexylpropanoic acid hydrate, Purity: 97%, CAS Number: 307310-72-1, Appearance: Form: solid, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 25g

Supplier: Thermo Scientific Chemicals
Description: N-Fmoc-D-alanine, 95%
Supplier: Ambeed
Description: N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-alanine hydrate 98% (by HPLC) (max.6% H₂O)

Supplier: TCI America
Description: CAS Number: 79990-15-1
MDL Number: MFCD00062960
Molecular Formula: C18H17NO4
Molecular Weight: 311.34
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Melting point (°C): 157
Specific rotation [a]20/D: 19 deg (C=1, DMF)

SDS

Supplier: Bachem Americas
Description: Sequence: Fmoc-D-Ala-OH · H₂O

Supplier: Matrix Scientific
Description: N-alpha-Fmoc-L-alanine

Supplier: Bachem Americas
Description: Sequence: Fmoc-Ala-OH · H₂O

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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.
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