2-Hydroxy-2-(trifluoromethyl)propionic+acid
Supplier:
TCI America
Description:
CAS Number: 4767-03-7
MDL Number: MFCD00004199 Molecular Formula: C5H10O4 Molecular Weight: 134.13 Purity/Analysis Method: >97.0% (T) Form: Crystal Boiling point (°C): 200 Melting point (°C): 185 Flash Point (°C): 220
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 006950-5G , MDL Number: MFCD00216521
Supplier:
Bachem Americas
Description:
Sequence: H-DL-β-(3,4-Dihydroxyphenyl)-DL-Ser-OH
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 041932-1G , MDL Number: MFCD00672555
Supplier:
Bachem Americas
Description:
Sequence: D-Lactic acid
Catalog Number:
(AAJ64508-03)
Supplier:
Thermo Scientific Chemicals
Description:
For iodination of proteins that do not contain tyrosine residues
Supplier:
AMBEED, INC
Description:
Methyl 3-oxo-3-(4-(trifluoromethyl)phenyl)propanoate, Purity: 98%, CAS number: 212755-76-5, Appearance: Pale yellow to pale yellow red powder or crystal, Storage: Sealed in dry, Room Temperature, Size: 100G
Catalog Number:
(82022-856)
Supplier:
G-Biosciences
Description:
G-Biosciences' Sulfo-SHPP (water-soluble Bolton-Hunter Reagent) is designed to aid the labeling of proteins with radioactive iodine
Supplier:
TCI America
Description:
CAS Number: 55-03-8
MDL Number: MFCD00002596 Molecular Formula: C15H11I4NO4 Molecular Weight: 798.86 Purity/Analysis Method: >98.0% (T) Form: Crystal Color: Very Pale Yellow Specific rotation [a]20/D: 16 deg (C=1, 1mol/L HCL:EtOH=1:4)
Catalog Number:
(103008-080)
Supplier:
Anaspec Inc
Description:
The synthetic peptide (Tat-Glur23Y) contains tyrosine residues that blocks phosphorylation of alpha-amino-3-hydroxy-5-methyl-isoxazole-4-propionic acid (AMPA) receptor endocytosis. Previous research shows that Tat-Glur23Y blocks regulated AMPA and thereby prevents long-term depression (LTD) in structures such as the nucleus accumbens and dorsal hippocampus.
Sequence: YGRKKRRQRRRYKEGYNVYG MW: 2634 Da % Peak area by HPLC: 95 Storage condition: -20°C
Catalog Number:
(PI27712)
Supplier:
Invitrogen
Description:
Sulfo-SHPP, sulfosuccinimidyl-3 -(4-hydroxypheynyl) propionate, also known as water-soluble Bolton-Hunter reagent, conjugates tyrosine-like functional groups to primary amines to increase the number of tyrosyl groups that can be iodinated by iodine-125 labeling procedures.
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 020549-5G , MDL Number: MFCD00002392
Catalog Number:
(103008-078)
Supplier:
Anaspec Inc
Description:
Tat-Glur23Y, scrambled is a control peptide. The synthetic peptide (Tat-Glur23Y), containing tyrosine residues, blocks phosphorylation of alpha-amino-3-hydroxy-5-methyl-isoxazole-4-propionic acid (AMPA) receptor endocytosis. However, the scrambled version does not have blockade properties. Previous studies show that Tat-Glur23Y, scrambled increase stress levels in mice, while Tat-Glur23Y reduces stress when administered.
Sequence: YGRKKRRQRRRVYKYGGYNE MW: 2634 Da % Peak area by HPLC: 95 Storage condition: -20°C
Supplier:
Invitrogen
Description:
Thermo Scientific Pierce DSP (Lomant's Reagent) is a water-insoluble, homo-bifunctional N-hydroxysuccimide ester (NHS ester) crosslinker that is thiol-cleavable, primary amine-reactive, and useful for many applications. DSP contains an amine-reactive NHS ester at each end of an 8-carbon spacer arm. NHS esters react with primary amines at pH 7–9 to form stable amide bonds and releasing N-hydroxy-succinimide. Proteins, including antibodies, generally have several primary amines in the side chain of lysine (K) residues and the N-terminus of each polypeptide that are available as targets for NHS ester crosslinking reagents. DSP is non-sulfonated and insoluble in water, so it must first be dissolved in an organic solvent and then added to the aqueous reaction mixture. Because DSP does not possess a charged group, it is lipophilic and membrane-permeable and so useful for intracellular and intramembrane conjugation. A sulfonated analog of DSP (DTTSP) is water soluble. DSS, the non-cleavable analog of the DSP crosslinker is also available for applications that require a stable spacer arm that cannot be cleaved in the presence of reducing agents.
Catalog Number:
(103523-924)
Supplier:
Invitrogen
Description:
Thermo Scientific Pierce DSP (Lomant's Reagent) is a water-insoluble, homo-bifunctional N-hydroxysuccimide ester (NHS ester) crosslinker that is thiol-cleavable, primary amine-reactive, and useful for many applications. DSP contains an amine-reactive NHS ester at each end of an 8-carbon spacer arm. NHS esters react with primary amines at pH 7–9 to form stable amide bonds and releasing N-hydroxy-succinimide. Proteins, including antibodies, generally have several primary amines in the side chain of lysine (K) residues and the N-terminus of each polypeptide that are available as targets for NHS ester crosslinking reagents. DSP is non-sulfonated and insoluble in water, so it must first be dissolved in an organic solvent and then added to the aqueous reaction mixture. Because DSP does not possess a charged group, it is lipophilic and membrane-permeable and so useful for intracellular and intramembrane conjugation. A sulfonated analog of DSP (DTTSP) is water soluble. DSS, the non-cleavable analog of the DSP crosslinker is also available for applications that require a stable spacer arm that cannot be cleaved in the presence of reducing agents.
Catalog Number:
(10075-718)
Supplier:
Prosci
Description:
The ion channels activated by glutamate are typically divided into two classes. Those that are sensitive to N-methyl-D-aspartate (NMDA) are designated NMDA receptors (NMDAR) while those activated by alpha-amino-3-hydroxy-5-methyl-4-isoxalone propionic acid (AMPA) are known as AMPA receptors (AMPAR). The AMPAR are comprised of four distinct Glutamate Receptor Subunits designated (GluR1-4) and they play key roles in virtually all excitatory neurotransmission in the brain (Keinänen et al., 1990;Hollmann and Heinemann, 1994). The GluR2 subunit is thought to play a key role in forms of synaptic plasticity such as LTD (Chung et al., 2003)
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