Benzyl+methyl+ether
Catalog Number:
(101813-818)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 022328-500MG , MDL Number: MFCD08687408
Catalog Number:
(101813-502)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 022170-500MG , MDL Number: MFCD08687411
Catalog Number:
(101826-536)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 028635-500MG , MDL Number: MFCD01990236
Catalog Number:
(101923-406)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 062157-500MG , MDL Number: MFCD12198029
Catalog Number:
(101815-650)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 023258-500MG , MDL Number: MFCD09879216
Catalog Number:
(101923-404)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 062156-500MG , MDL Number: MFCD12198028
Catalog Number:
(101826-326)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 028532-500MG , MDL Number: MFCD02629610
Catalog Number:
(101815-096)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 022971-500MG , MDL Number: MFCD08687801
Catalog Number:
(101923-172)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 062040-500MG , MDL Number: MFCD12197918
Catalog Number:
(101923-252)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 062080-500MG , MDL Number: MFCD12197956
Catalog Number:
(101892-418)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 050629-2.5G , MDL Number: MFCD13561025
Catalog Number:
(10318-338)
Supplier:
Bioss
Description:
C9orf163 (chromosome 9 open reading frame 163) is a 203 amino acid protein encoded by a gene that maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Catalog Number:
(10314-304)
Supplier:
Bioss
Description:
C9orf21 (chromosome 9 open reading frame 21) is a 226 amino acid protein that belongs to the UPF0308 family and is encoded by a gene that maps to human chromosome 9q22.33. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Supplier:
AMBEED, INC
Description:
3-((Dimethyl(vinyl)silyl)oxy)-1,1,3,5,5-pentamethyl-1,5-divinyltrisiloxane, Purity: 95% mix TBC as stabilizer, CAS Number: 60111-52-6, Appearance: Liquid, Storage: Inert atmosphere, 2-8C, Size: 5G
Catalog Number:
(101930-342)
Supplier:
Matrix Scientific
Description:
MF=C9H16N2O MW=168.24 MDL=MFCD19103485 500Mg
Catalog Number:
(101826-544)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 028639-500MG , MDL Number: MFCD03422473
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