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Supplier: TCI America
Description: CAS Number: 516-05-2
MDL Number: MFCD00002656
Molecular Formula: C4H6O4
Molecular Weight: 118.09
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Melting point (°C): 135
Supplier: TCI America
Description: CAS Number: 609-08-5
MDL Number: MFCD00009162
Molecular Formula: C8H14O4
Molecular Weight: 174.20
Purity/Analysis Method: >98.0% (GC)
Form: Clear Liquid
Boiling point (°C): 199
Flash Point (°C): 82
Specific Gravity (20/20): 1.02
Supplier: Thermo Scientific Chemicals
Description: Diethyl-2-bromo-2-methylmalonate 98%
Catalog Number: (76576-574)
Supplier: AFG BIOSCIENCE LLC
Description: Human Methylmalonic Acid (MMA) ELISA Kit, AFG Bioscience


Supplier: TCI America
Description: CAS Number: 2049-70-9
MDL Number: MFCD02258541
Molecular Formula: C10H18O4
Molecular Weight: 202.25
Purity/Analysis Method: >97.0% (GC)
Form: Clear Liquid
Boiling point (°C): 79
Specific Gravity (20/20): 0.99

SDS

Catalog Number: (77526-396)
Supplier: AFG BIOSCIENCE LLC
Description: Human MMA (Methylmalonic Acid) ELISA Kit

New Product


Catalog Number: (77510-608)
Supplier: AFG BIOSCIENCE LLC
Description: Mouse MMA (Methylmalonic Acid) ELISA Kit

New Product


Catalog Number: (89424-106)
Supplier: Genetex
Description: Rabbit Polyclonal antibody to MMAB (methylmalonic aciduria (cobalamin deficiency) cblB type)


Catalog Number: (76120-824)
Supplier: Bioss
Description: C2ORF25 is a mitochondrial protein and its function is not fully identified. But, Vitamin B12 (cobalamin) is an essential cofactor in several metabolic pathways. Intracellular conversion of cobalamin to adenosylcobalamin in mitochondria and to methylcobalamin in cytoplasm is necessary for homeostasis of methylmalonic acid and homocysteine. C2ORF25 encodes a protein involved in an early step of cobalamin metabolism.


Catalog Number: (76120-822)
Supplier: Bioss
Description: C2ORF25 is a mitochondrial protein and its function is not fully identified. But, Vitamin B12 (cobalamin) is an essential cofactor in several metabolic pathways. Intracellular conversion of cobalamin to adenosylcobalamin in mitochondria and to methylcobalamin in cytoplasm is necessary for homeostasis of methylmalonic acid and homocysteine. C2ORF25 encodes a protein involved in an early step of cobalamin metabolism.


Catalog Number: (10104-316)
Supplier: Prosci
Description: The function of C2orf25 remains unknown.Vitamin B12 (cobalamin) is an essential cofactor in several metabolic pathways. Intracellular conversion of cobalamin to adenosylcobalamin in mitochondria and to methylcobalamin in cytoplasm is necessary for homeostasis of methylmalonic acid and homocysteine. C2ORF25 encodes a protein involved in an early step of cobalamin metabolism (Coelho et al., 2008 [PubMed 18385497]).


Catalog Number: (76100-040)
Supplier: Bioss
Description: HIBADH is a 336 amino acid mitochondrial enzyme that catalyzes the NAD+-dependent, reversible oxidization of 3-Hydroxyisobutyrate to methylmalonate semialdehyde, an intermediate of valine catabolism. The enzyme functions as a homodimer between a pH of 7.0 and 10.0, with optimal activity between 8.8 and 9.0. It was previously hypothesized that defects in the gene encoding HIBADH may be the cause of 3-Hydroxyisobutyric aciduria, a rare disorder that is characterized by a variety of clinical manifestations such as neurodevelopmental problems and dysmorphic features. However, it was shown that HIBADH activity was equal in patients with 3-Hydroxyisobutyric aciduria as compared with controls.


Catalog Number: (76100-038)
Supplier: Bioss
Description: HIBADH is a 336 amino acid mitochondrial enzyme that catalyzes the NAD+-dependent, reversible oxidization of 3-Hydroxyisobutyrate to methylmalonate semialdehyde, an intermediate of valine catabolism. The enzyme functions as a homodimer between a pH of 7.0 and 10.0, with optimal activity between 8.8 and 9.0. It was previously hypothesized that defects in the gene encoding HIBADH may be the cause of 3-Hydroxyisobutyric aciduria, a rare disorder that is characterized by a variety of clinical manifestations such as neurodevelopmental problems and dysmorphic features. However, it was shown that HIBADH activity was equal in patients with 3-Hydroxyisobutyric aciduria as compared with controls.


Catalog Number: (76099-062)
Supplier: Bioss
Description: C4orf17 (chromosome 4 open reading frame 17) is a 359 amino acid protein encoded by a gene that maps to human chromosome 4. Human chromosome 4 represents approximately 6% of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded by a gene that is located on chromosome 4, and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.


Catalog Number: (76099-074)
Supplier: Bioss
Description: C4orf29 (chromosome 4 open reading frame 29) is a 414 amino acid secreted protein that exists as four alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 4. Human chromosome 4 represents approximately 6% of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is located on chromosome 4. FGFR-3 is also encoded by a gene that maps to human chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.


Catalog Number: (76099-064)
Supplier: Bioss
Description: C4orf17 (chromosome 4 open reading frame 17) is a 359 amino acid protein encoded by a gene that maps to human chromosome 4. Human chromosome 4 represents approximately 6% of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded by a gene that is located on chromosome 4, and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.


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