You Searched For: 12-Aminolauric+acid


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Supplier: Zymo Research
Description: Swab collection system with tubes pre-filled with DNA/RNA Shield™ for collection and stabilization of nucleic acid at room termperature.

Supplier: Chemglass
Description: Brown, low compression, 75 durometer Viton® O-rings are suitable for acids, aliphatic hydrocarbons, oxidizing agents, and all petroleum products

Small Business Enterprise

Supplier: MilliporeSigma
Description: Flammable.
Supplier: Thermo Scientific Chemicals
Description: EDTA tripotassium salt dihydrate 99%
Supplier: AVANTOR PERFORMANCE MATERIAL LLC
Description: N,N-Dimethylformamide, J.T.Baker®

Supplier: TCI America
Description: CAS Number: 84348-37-8
MDL Number: MFCD01860669
Molecular Formula: C10H15NO5
Molecular Weight: 229.23
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Melting point (°C): 158
Specific rotation [a]20/D: 20 deg (C=0.5, Acetone)
Storage Temperature: 0-10°C

SDS

Catalog Number: (89419-540)
Supplier: Prosci
Description: LGP2 peptide is used for blocking the activity of LGP2 antibody.


Supplier: TCI America
Description: [for Biochemical Research]
CAS Number: 6381-92-6
MDL Number: MFCD00150037
Molecular Formula: C10H16N2O8
Molecular Weight: 336.21
Purity/Analysis Method: >99.0% (T)
Form: Crystal
Melting point (°C): 252
Catalog Number: (10390-292)
Supplier: Bioss
Description: Acyl-CoA synthetase probably involved in bile acid metabolism. Proposed to activate C27 precurors of bile acids to their CoA thioesters derivatives before side chain cleavage via peroxisomal beta-oxidation occurs. In vitro, activates 3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholestanate (THCA), the C27 precursor of cholic acid deriving from the de novo synthesis from cholesterol. Does not utilize C24 bile acids as substrates. In vitro, also activates long- and branched-chain fatty acids and may have additional roles in fatty acid metabolism. May be involved in translocation of long-chain fatty acids (LFCA) across membranes (By similarity).


Catalog Number: (10390-284)
Supplier: Bioss
Description: Acyl-CoA synthetase probably involved in bile acid metabolism. Proposed to activate C27 precurors of bile acids to their CoA thioesters derivatives before side chain cleavage via peroxisomal beta-oxidation occurs. In vitro, activates 3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholestanate (THCA), the C27 precursor of cholic acid deriving from the de novo synthesis from cholesterol. Does not utilize C24 bile acids as substrates. In vitro, also activates long- and branched-chain fatty acids and may have additional roles in fatty acid metabolism. May be involved in translocation of long-chain fatty acids (LFCA) across membranes (By similarity).


Catalog Number: (10390-288)
Supplier: Bioss
Description: Acyl-CoA synthetase probably involved in bile acid metabolism. Proposed to activate C27 precurors of bile acids to their CoA thioesters derivatives before side chain cleavage via peroxisomal beta-oxidation occurs. In vitro, activates 3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholestanate (THCA), the C27 precursor of cholic acid deriving from the de novo synthesis from cholesterol. Does not utilize C24 bile acids as substrates. In vitro, also activates long- and branched-chain fatty acids and may have additional roles in fatty acid metabolism. May be involved in translocation of long-chain fatty acids (LFCA) across membranes (By similarity).


Supplier: Thermo Scientific Chemicals
Description: MDL: MFCD00042553 Practically insoluble in water, acetone, and glacial acetic acid
Catalog Number: (TCD2456-025G)
Supplier: TCI America
Description: CAS Number: 35466-87-6
MDL Number: MFCD00460005
Molecular Formula: C8H14O6
Molecular Weight: 206.19
Purity/Analysis Method: >98.0% (GC)
Form: Clear Liquid
Boiling point (°C): 227
Specific Gravity (20/20): 1.15

Supplier: TCI America
Description: CAS Number: 213178-94-0
MDL Number: MFCD00217056
Molecular Formula: C9H17NO2
Molecular Weight: 171.24
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Specific rotation [a]20/D: -12 deg (C=1, 1mol/L HCl)

SDS

Supplier: Thermo Scientific Chemicals
Description: Methyl cholate 98+%
Catalog Number: (10473-614)
Supplier: Bioss
Description: Catalyzes the NADPH-dependent reduction of a variety of aromatic and aliphatic aldehydes to their corresponding alcohols. Catalyzes the reduction of mevaldate to mevalonic acid and of glyceraldehyde to glycerol. Has broad substrate specificity. In vitro substrates include succinic semialdehyde, 4-nitrobenzaldehyde, 1,2-naphthoquinone, methylglyoxal, and D-glucuronic acid. Plays a role in the activation of procarcinogens, such as polycyclic aromatic hydrocarbon trans-dihydrodiols, and in the metabolism of various xenobiotics and drugs, including the anthracyclines doxorubicin (DOX) and daunorubicin (DAUN).


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