41323 Results for: "2-Amino-5,6-dimethlbenzothiazole"

Supplier: Abgent

Polyclonal antibody, Isotype: Rabbit Ig, Species Reactivity: Human, Gene ID: 18708, Target/Specificity: Generated from rabbits immunized with a KLH conjugated synthetic peptide between 56-84 amino acids from the N-terminal region of mouse Pik3r1.

Supplier: Abgent

Polyclonal antibody, Isotype: Rabbit Ig, Species Reactivity: Human, Gene ID: 8676, Target/Specificity: Generated from rabbits immunized with a KLH conjugated synthetic peptide between 29-56 amino acids from the N-terminal region of human STX11.

Supplier: Abgent

Polyclonal antibody, Isotype: Rabbit Ig species reactivity: human , Gene ID: 51052, Target/Specificity: generated from rabbits immunized with a KLH conjugated synthetic peptide between 27-56 amino acids from the Central region of human PRLH.

Supplier: Abgent

Polyclonal Antibody, Isotype: Rabbit Ig, Species Reactivity: Human, Gene ID: 9144, Target/Specificity: generated from rabbits immunized with a KLH conjugated synthetic peptide between 28-56 amino acids from the N-terminal region of human SYNGR2

Supplier: Abgent

Polyclonal Antibody, Host: , Isotype: Rabbit Ig, Species Reactivity: Human, Gene ID: 26257, Target/Specificity: generated from rabbits immunized with a KLH conjugated synthetic peptide between 30-56 amino acids from the N-terminal region of human NKX2-8.

Supplier: MilliporeSigma

Cas Number 56-45-1, For Synthesis

Supplier: Abgent

Monoclonal antibody Clone: 557CT5.2.1 , Host: mouse , Isotype: IgG2b, species reactivity: human , Gene ID: 581, Target/Specificity: generated from mice immunized with a KLH conjugated synthetic peptide between 28-56 amino acids from human BAX.

Supplier: Abgent

Polyclonal antibody, Isotype: Rabbit Ig, Species reactivity: Human, Gene ID: 5463, Target/Specificity: This POU6F1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 56-85 amino acids from the N-terminal region of human POU6F1.

Supplier: Abgent

Polyclonal Antibody Reactivity: Human, Isotype: Rabbit Ig, Gene ID: 2653, Target/Specificity: generated from rabbits immunized with a KLH conjugated synthetic peptide between 27-56 amino acids from the N-terminal region of human GCSH

Supplier: Abgent

Polyclonal antibody, Isotype: Rabbit Ig, Species Reactivity: Human , Gene ID: 3597, Target/Specificity: generated from rabbits immunized with a KLH conjugated synthetic peptide between 56-85 amino acids from the N-terminal region of human IL13RA1

Supplier: Abgent

Polyclonal antibody, Isotype: Rabbit Ig, Species Reactivity: Human, Gene ID: 2182, Target/Specificity: Generated from rabbits immunized with a KLH conjugated synthetic peptide between 28-56 amino acids from the N-terminal region of human ACSL4.

Supplier: Abgent

Polyclonal Antibody, Isotype: Rabbit Ig, Species Reactivity: Human, Gene ID: 259215, Target/Specificity: generated from rabbits immunized with a KLH conjugated synthetic peptide between 56-84 amino acids from the N-terminal region of human LY6G6F

Supplier: Abgent

Polyclonal Antibody, Host: , Isotype: Rabbit Ig, Species Reactivity: Human, Gene ID: 10368, Target/Specificity: generated from rabbits immunized with a KLH conjugated synthetic peptide between 28-56 amino acids from the N-terminal region of human CACNG3.

Supplier: Genetex

Rabbit Polyclonal antibody to ATP6V1B2 (ATPase, H+ transporting, lysosomal 56/58kDa, V1 subunit B2)

Supplier: TCI America

CAS Number: 32986-56-4
MDL Number: MFCD00077885
Molecular Formula: C18H37N5O9
Molecular Weight: 467.52
Purity/Analysis Method: >94.0% (T)
Form: Crystal
Color: White
Melting point (°C): 178
Specific rotation [a]20/D: 143 deg (C=4, H2O)

Supplier: Abgent

Polyclonal Antibody, Species Reactivity: Rat, Isotype: Rabbit Ig, Gene ID: 497985, Target/Specificity: This Rat Hoxb7 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 56-83 amino acids from the Central region of rat Hoxb7, 1mg

Supplier: Bioss

Catalyzes the second step of the reductive pyrimidine degradation, the reversible hydrolytic ring opening of dihydropyrimidines. Can catalyzes the ring opening of 5,6-dihydrouracil to N-carbamyl-alanine and of 5,6-dihydrothymine to N-carbamyl-amino isobutyrate.Tissue specificity:Liver and kidney.Involvement in disease:Defects in DPYS are the cause of dihydropyrimidinase deficiency (DHPD). DHPD is an autosomal recessive disorder characterized by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features and severe developmental delay, and congenital microvillous atrophy.

Supplier: Bioss

Catalyzes the second step of the reductive pyrimidine degradation, the reversible hydrolytic ring opening of dihydropyrimidines. Can catalyzes the ring opening of 5,6-dihydrouracil to N-carbamyl-alanine and of 5,6-dihydrothymine to N-carbamyl-amino isobutyrate.Tissue specificity:Liver and kidney.Involvement in disease:Defects in DPYS are the cause of dihydropyrimidinase deficiency (DHPD). DHPD is an autosomal recessive disorder characterized by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features and severe developmental delay, and congenital microvillous atrophy.

Supplier: MilliporeSigma

Cas Number 56-85-9, For Synthesis

Supplier: AVANTOR PERFORMANCE MATERIAL LLC

Supplier: Bioss

Catalyzes the second step of the reductive pyrimidine degradation, the reversible hydrolytic ring opening of dihydropyrimidines. Can catalyzes the ring opening of 5,6-dihydrouracil to N-carbamyl-alanine and of 5,6-dihydrothymine to N-carbamyl-amino isobutyrate.Tissue specificity:Liver and kidney.Involvement in disease:Defects in DPYS are the cause of dihydropyrimidinase deficiency (DHPD). DHPD is an autosomal recessive disorder characterized by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features and severe developmental delay, and congenital microvillous atrophy.

Supplier: Bioss

Catalyzes the second step of the reductive pyrimidine degradation, the reversible hydrolytic ring opening of dihydropyrimidines. Can catalyzes the ring opening of 5,6-dihydrouracil to N-carbamyl-alanine and of 5,6-dihydrothymine to N-carbamyl-amino isobutyrate.Tissue specificity:Liver and kidney.Involvement in disease:Defects in DPYS are the cause of dihydropyrimidinase deficiency (DHPD). DHPD is an autosomal recessive disorder characterized by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features and severe developmental delay, and congenital microvillous atrophy.

Supplier: Bioss

Catalyzes the second step of the reductive pyrimidine degradation, the reversible hydrolytic ring opening of dihydropyrimidines. Can catalyzes the ring opening of 5,6-dihydrouracil to N-carbamyl-alanine and of 5,6-dihydrothymine to N-carbamyl-amino isobutyrate.Tissue specificity:Liver and kidney.Involvement in disease:Defects in DPYS are the cause of dihydropyrimidinase deficiency (DHPD). DHPD is an autosomal recessive disorder characterized by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features and severe developmental delay, and congenital microvillous atrophy.

Supplier: Bioss

Catalyzes the second step of the reductive pyrimidine degradation, the reversible hydrolytic ring opening of dihydropyrimidines. Can catalyzes the ring opening of 5,6-dihydrouracil to N-carbamyl-alanine and of 5,6-dihydrothymine to N-carbamyl-amino isobutyrate.Tissue specificity:Liver and kidney.Involvement in disease:Defects in DPYS are the cause of dihydropyrimidinase deficiency (DHPD). DHPD is an autosomal recessive disorder characterized by dihydropyrimidinuria and associated with a variable clinical phenotype: epileptic or convulsive attacks, dysmorphic features and severe developmental delay, and congenital microvillous atrophy.

Supplier: MilliporeSigma

Cas Number 56-84-8, For Synthesis

Supplier: Biotium

CBQCA (3-(4-carboxybenzoyl)quinoline-2-carboxaldehyde) reacts specifically with primary amines to form conjugates that can be analyzed by electrophoretic or chromatographic methods. CBQCA also reacts with hydrophilic peptides and amino sugars. The amine derivatized product (7-aza-1-cyano-5,6-benzisoindole) is highly fluorescent that is optimally excited at 450 nm and have emission maximum at 560 nm.

Supplier: Bioss

The protein encoded by this gene is a member of the kelch family of proteins, which is characterized by a 44-56 amino acid repeat motif. The kelch motif appears in many different polypeptide contexts and contains multiple potential protein-protein contact sites. Members of this family are present both throughout the cell and extracellularly, with diverse activities.

Supplier: Abgent

Western Blot: 1:100~250,

Supplier: Spectrum Chemicals

L-Glutamine, FCC - The FCC grade meets the requirements of the Food Chemical Codex indicates and is suitable for all food, beverage and nutritional supplement applications. Spectrum Chemical offers over 300 Food grade chemical ingredients packaged in laboratory size bottles to production drum quantities and are manufactured, packaged and stored under current Good Manufacturing Practices (cGMP) per 21CFR part 211 in FDA registered and inspected facilities.

Supplier: TCI America

CAS Number: 118399-28-3
MDL Number: MFCD09839299
Molecular Formula: C12H13NO4
Molecular Weight: 235.24
Purity/Analysis Method: >98.0% (HPLC,N)
Form: Crystal
Melting point (°C): 107
Specific rotation [a]20/D: 56 deg (C=1, CHCl3)