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2,4-Difluoro-3-(methylthio)benzoic+acid
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2,4-Difluoro-3-(methylthio)benzoic+acid
Supplier:
AOB CHEM USA
Description:
(3-Ethoxy-2-fluoro-5-iodophenyl)boronic acid ≥97%
Supplier:
AMBEED, INC
Description:
2-(2-Ethoxy-4-formylphenoxy)acetic acid, Purity: 97%, CAS Number: 51264-76-7, Appearance: White to off-white solid, Storage: Inert atmosphere, 2-8 C, Size: 5g
Catalog Number:
(10476-016)
Supplier:
Bioss
Description:
PLEKHM3 (pleckstrin homology domain containing, family M, member 3), also known as DAPR or PLEKHM1L (pleckstrin homology domain containing, family M, member 1-like), is a 761 amino acid phosphoprotein that contains two pleckstrin homology (PH) domains and one phorbol-ester/DAG-type zinc finger. Conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, PLEKHM3 exists as three alternatively spliced isoforms that participate in metal ion binding. The gene that encodes PLEKHM3 maps to human chromosome 2q33.3. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. Chromosome 2 contains a probable vestigial second centromere, as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.
Catalog Number:
(10476-018)
Supplier:
Bioss
Description:
PLEKHM3 (pleckstrin homology domain containing, family M, member 3), also known as DAPR or PLEKHM1L (pleckstrin homology domain containing, family M, member 1-like), is a 761 amino acid phosphoprotein that contains two pleckstrin homology (PH) domains and one phorbol-ester/DAG-type zinc finger. Conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, PLEKHM3 exists as three alternatively spliced isoforms that participate in metal ion binding. The gene that encodes PLEKHM3 maps to human chromosome 2q33.3. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. Chromosome 2 contains a probable vestigial second centromere, as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.
Supplier:
AOB CHEM USA
Description:
(2-Ethoxy-3-(tert-pentyl)phenyl)boronic acid ≥95%
Supplier:
Thermo Scientific Chemicals
Description:
1g CAS: 126617-98-9, MDL: MFCD03412110
Catalog Number:
(10266-442)
Supplier:
Bioss
Description:
Sulfatases are enzymes that hydrolyse a diverse range of sulfate esters. Deficiency of lysosomal sulfatases leads to human diseases characterized by the accumulation of either GAGs (glycosaminoglycans) or sulfolipids. Sulfamidase, also known as HSS, SFMD, MPS3A or SGSH, is a 502 amino acid lysosome that belongs to the sulfatase family. It has been suggested that sulfamidase may be involved in the lysosomal degradation of heparan sulfate. Defects in the gene encoding sulfamidase are the cause of Sanfilippo syndrome A, an autosomal recessive lysosomal storage disease caused by impaired degradation of heparan sulfate. Sanfilippo syndrome A is characterized by severe central nervous system degeneration but relatively mild somatic manifestations.
Supplier:
AOB CHEM USA
Description:
3-Bromo-4-ethoxy-2-fluorobenzoic acid ≥97%
Supplier:
AOB CHEM USA
Description:
2-Ethoxy-3-fluoro-5-methylbenzoic acid ≥97%
Catalog Number:
(10266-450)
Supplier:
Bioss
Description:
Sulfatases are enzymes that hydrolyse a diverse range of sulfate esters. Deficiency of lysosomal sulfatases leads to human diseases characterized by the accumulation of either GAGs (glycosaminoglycans) or sulfolipids. Sulfamidase, also known as HSS, SFMD, MPS3A or SGSH, is a 502 amino acid lysosome that belongs to the sulfatase family. It has been suggested that sulfamidase may be involved in the lysosomal degradation of heparan sulfate. Defects in the gene encoding sulfamidase are the cause of Sanfilippo syndrome A, an autosomal recessive lysosomal storage disease caused by impaired degradation of heparan sulfate. Sanfilippo syndrome A is characterized by severe central nervous system degeneration but relatively mild somatic manifestations.
Supplier:
AMBEED, INC
Description:
(4-Ethoxy-2,6-difluorophenyl)boronic acid, Purity: 97%, CAS number: 1310403-94-1, Appearance: White to off-white powder or crystals, Storage: Inert atmosphere, 2-8C, Size: 250MG
Supplier:
AMBEED, INC
Description:
(2-Formyl-5-(trifluoromethyl)phenyl)boronic acid, Purity: 95+%, CAS Number: 1204580-94-8, Appearance: Solid, Storage: Inert atmosphere, 2-8C, Size: 100MG
Supplier:
AMBEED, INC
Description:
(3-Bromo-2-ethoxy-5-fluorophenyl)boronic acid 95%
Supplier:
AMBEED, INC
Description:
(3-Chloro-4-ethoxy-5-fluorophenyl)boronic acid, Purity: 97%, CAS Number: 2096334-30-2, Appearance: Solid, Storage: Inert atmosphere, 2-8 deg C, Size: 250mg
Catalog Number:
(101848-752)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 040057-500MG , MDL Number: MFCD09870332
Supplier:
Matrix Scientific
Description:
2-Ethoxy-5-iodonicotinic acid ≥97%
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