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Methyl+2-amino-3,5-difluorobenzoate
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Methyl+2-amino-3,5-difluorobenzoate
Supplier:
Matrix Scientific
Description:
MF=C8H10N5NAO3 MW=247.19 CAS=69657-51-8 MDL=MFCD01694138 1G
Catalog Number:
(10480-156)
Supplier:
Bioss
Description:
DHRS1 (dehydrogenase/reductase (SDR family) member 1), also known as SDR19C1, is a 313 amino acid protein that belongs to the short-chain dehydrogenases/reductases (SDR) family and likely functions as an oxidoreductase. Abundantly expressed in heart and liver, DHRS1 contains an SDR motif and is encoded by a gene that maps to human chromosome 14q12. Human chromosome 14 houses over 700 genes and comprises nearly 3.5% of the human genome. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease (AD). The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder ?-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction.
Supplier:
AMBEED, INC
Description:
2-(4-(((tert-Butoxycarbonyl)amino)methyl)phenyl)acetic acid, Purity: 98%, CAS Number: 71420-92-3, Appearance: White to Yellow Solid, Storage: Sealed in dry, 2-8 C, Size: 1g
Supplier:
ALADDIN SCIENTIFIC
Description:
5-Amino-2-methylbenzoic acid ≥97%
Catalog Number:
(10483-874)
Supplier:
Bioss
Description:
GLB1L3 is a 653 amino acid protein belonging to the glycosyl hydrolase 35 family. GLB1L3 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q25. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
Supplier:
AMBEED, INC
Description:
(R)-2-Amino-1-ethyl-7-(3-hydroxy-4-methoxy-3-methylbut-1-yn-1-yl)-N-methyl-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxamide, Purity: 98%, CAS Number: 1433953-83-3, Appearance: Solid, Storage: Keep in dark place, Inert atmosphere, Store in freezer, under -20 C, Size: 10mg
Supplier:
BeanTown Chemical
Description:
CAS: 147118-36-3; MDL No: MFCD08063917
Solid; Molecular Formula: C16H20FN3O3S; MW: 353.41
Supplier:
AMBEED, INC
Description:
[2'-(Amino-KN)[1,1'-biphenyl]-2-yl-KC][bis(1,1-dimethylethyl)[3-methoxy-6-methyl-2',4',6'-tris(1-methylethyl)[1,1'-biphenyl]-2-yl]phosphine-KP](methanesulfonato-KO)palladium, Purity: 98%, CAS Number: 2009020-38-4, Appearance: Solid, Storage: Keep in dark place, Inert atmosphere, 2-8C, Size: 5G
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 059159-1G , MDL Number: MFCD00126682
Supplier:
TCI America
Description:
CAS Number: 59277-89-3
Molecular Formula: C8H11N5O3 Molecular Weight: 225.21 Purity/Analysis Method: >98.0% (HPLC) Form: Crystal Melting point (°C): 262
Supplier:
AMBEED, INC
Description:
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-fluorophenyl)-2-methylpropanoic acid, Purity: 95%, CAS Number: 1172127-44-4, Appearance: White to off white to light-green powder or crystals, Storage: Sealed in dry, 2-8 C, Size: 5g
Catalog Number:
(77627-688)
Supplier:
AMBEED, INC
Description:
2-Methyl-5-isopropylaniline ≥97%
Supplier:
AMBEED, INC
Description:
4-Methyl-3-(2-((2-morpholinoethyl)amino)quinazolin-6-yl)-N-(3-(trifluoromethyl)phenyl)benzamide, Purity: 98%, CAS Number: 882663-88-9, Appearance: Pale-yellow or Pale red to Yellow-brown Solid, Storage: Keep in dark place, Sealed in dry, 2-8 C, Size: 1mg
Catalog Number:
(76108-806)
Supplier:
Bioss
Description:
GLB1L3 is a 653 amino acid protein belonging to the glycosyl hydrolase 35 family. GLB1L3 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q25. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
Supplier:
AMBEED, INC
Description:
Calpeptin 98%
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
is still displayed and you need assistance, please call us at 1-800-932-5000.
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