You Searched For: Glycine

Catalog Number: (SCUE70000184)

Supplier: SCHUELKE MAYR

Description: Liquid concentrate based on quaternary ammonium, aromatic alcohols, non ionic surfactants and amphoteric glycine derivative suitable for surface cleaning and disinfection.

UOM: 1 * 5 L

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Supplier: MP Biomedicals

Description: Synthetic Bactericidal Antibiotic. A structural analog of D-Alanine. A partial agonist at the glycine modulatory site of NMDA receptors; enhances learning and memory in several models of cognitive deficit; anticonvulsant (at high doses). Antibiotic against gram-negative bacteria that acts by inhibiting the synthesis of the cell wall (D-Ala peptide bond formation).

Catalog Number: (USBI137834)

Supplier: US Biological

Description: Anti-CFB Goat Polyclonal Antibody

UOM: 1 * 1 mg

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Catalog Number: (BOSSBS-2970R-CY7)

Supplier: Bioss

Description: The survival and development of central neurons require the supply of trophic factors by glial cells. The trophic actions of glial cells on Purkinje neurons are mediated by L-serine and glycine, which are glia-derived trophic factors synthesized by 3PGDH (1). 3PGDH protein is 544 amino acids in length. Two distinct mRNA transcripts that encode for 3PGDH protein in normal human tissues are dominant 2.1 kb mRNA, which is highly expressed in prostate, testis, ovary, brain, liver, kidney, and pancreas, and weakly expressed in thymus, colon, and heart, and 710 bp mRNA, which is highly expressed in heart and skeletal muscle (2). 3PGDH is regulated at the transcriptional level depending on tissue specificity and cellular proliferative status (2). 3PGDH protein is also highly expressed in adult and fetal brain tissues (3). 3PGDH protein plays an important role in the metabolism, development, and function of the central nervous system (3) and its deficiency is a treatable congential error (4-5) that impairs L-serine biosynthesis which is characterized by congenital microcephaly, psychomotor retardation, and seizures (3).

UOM: 1 * 100 µl

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Catalog Number: (BOSSBS-2970R-FITC)

Supplier: Bioss

Description: The survival and development of central neurons require the supply of trophic factors by glial cells. The trophic actions of glial cells on Purkinje neurons are mediated by L-serine and glycine, which are glia-derived trophic factors synthesized by 3PGDH (1). 3PGDH protein is 544 amino acids in length. Two distinct mRNA transcripts that encode for 3PGDH protein in normal human tissues are dominant 2.1 kb mRNA, which is highly expressed in prostate, testis, ovary, brain, liver, kidney, and pancreas, and weakly expressed in thymus, colon, and heart, and 710 bp mRNA, which is highly expressed in heart and skeletal muscle (2). 3PGDH is regulated at the transcriptional level depending on tissue specificity and cellular proliferative status (2). 3PGDH protein is also highly expressed in adult and fetal brain tissues (3). 3PGDH protein plays an important role in the metabolism, development, and function of the central nervous system (3) and its deficiency is a treatable congential error (4-5) that impairs L-serine biosynthesis which is characterized by congenital microcephaly, psychomotor retardation, and seizures (3).

UOM: 1 * 100 µl

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Catalog Number: (USBI037996-BIOTIN)

Supplier: US Biological

Description: Anti-LSM4 Rabbit Polyclonal Antibody (Biotin)

UOM: 1 * 200 µl

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Catalog Number: (50018.)

Supplier: Biotium

Description: Membrane-permeant form of Fluo-4 calcium indicator.

UOM: 1 * 10 items

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Catalog Number: (PRSI56-326)

Supplier: ProSci Inc.

Description: GRIN3B is a NMDA receptor subtype of glutamate-gated ion channels with reduced single-channel conductance, low calcium permeability and low voltage-dependent sensitivity to magnesium. It is mediated by glycine.

UOM: 1 * 400 µl

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Supplier: Thermo Fisher Scientific

Description: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)decanoic acid 98% (by HPLC)

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Catalog Number: (PRSI26-066)

Supplier: ProSci Inc.

Description: BAAT is a liver enzyme that catalyzes the transfer of C24 bile acids from the acyl-CoA thioester to either glycine or taurine, the second step in the formation of bile acid-amino acid conjugates. The bile acid conjugates then act as a detergent in the gastrointestinal tract, which enhances lipid and fat-soluble vitamin absorption. Defects in this gene are a cause of familial hypercholanemia (FHCA). The protein encoded by this gene is a liver enzyme that catalyzes the transfer of C24 bile acids from the acyl-CoA thioester to either glycine or taurine, the second step in the formation of bile acid-amino acid conjugates. The bile acid conjugates then act as a detergent in the gastrointestinal tract, which enhances lipid and fat-soluble vitamin absorption. Defects in this gene are a cause of familial hypercholanemia (FHCA). Two transcript variants encoding the same protein have been found for this gene.

UOM: 1 * 50 µG

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Supplier: AAT BIOQUEST

Description: Calcium measurement is critical for numerous biological investigations.

Catalog Number: (PRSI29-236)

Supplier: ProSci Inc.

Description: RBMY1A1 is a protein containing an RNA-binding motif in the N-terminus and four SRGY (serine, arginine, glycine, tyrosine) boxes in the C-terminus. The gene that encodes RBMY1A1 is Y-linked. RBMY1A1 may be involved in spermatogenesis. It is required for sperm development, possibly by participating in pre-mRNA splicing in the testis.

UOM: 1 * 50 µG

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Catalog Number: (PRSI27-169)

Supplier: ProSci Inc.

Description: DLD is the L protein of the mitochondrial glycine cleavage system. The L protein, also named dihydrolipoamide dehydrogenase, is also a component of the pyruvate dehydrogenase complex, the alpha-ketoglutarate dehydrogenase complex, and the branched-chain alpha-keto acide dehydrogenase complex. Mutations in this gene have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency.This gene encodes the L protein of the mitochondrial glycine cleavage system. The L protein, also named dihydrolipoamide dehydrogenase, is also a component of the pyruvate dehydrogenase complex, the alpha-ketoglutarate dehydrogenase complex, and the branched-chain alpha-keto acide dehydrogenase complex. Mutations in this gene have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

UOM: 1 * 50 µG

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Catalog Number: (AGRIAS05074)

Supplier: Agrisera

Description: Anti-GDC-H Rabbit Polyclonal Antibody

UOM: 1 * 50 µG

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Catalog Number: (ROCK600-401-D65)

Supplier: Rockland Immunochemicals

Description: Anti-Glycine Receptor (Rabbit) antibody is suitable for use in Western Blotting and IHC. Specific conditions for reactivity should be optimized by the end user. Expect a band of approximately 48 kDa in size corresponding to the alpha 1 and alpha 2 subunit of the GABA(A) Receptor.

UOM: 1 * 200 µG

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Catalog Number: (PRSI31-356)

Supplier: ProSci Inc.

Description: USP48 is a protein containing domains that associate it with the peptidase family C19, also known as family 2 of ubiquitin carboxyl-terminal hydrolases. Family members function as deubiquitinating enzymes, recognizing and hydrolyzing the peptide bond at the C-terminal glycine of ubiquitin. Enzymes in peptidase family C19 are involved in the processing of poly-ubiquitin precursors as well as that of ubiquitinated proteins.

UOM: 1 * 100 µG

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