2-(4-Chlorophenyl)-2,2-difluoroacetic+acid
Catalog Number:
(101842-534)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 037031-500MG , MDL Number: MFCD00022562
Supplier:
AOB CHEM USA
Description:
(3-Chlorophenyl)(furan-2-yl)methanol ≥97%
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 044222-5G , MDL Number: MFCD01045654
Supplier:
AMBEED, INC
Description:
Methyl-2-amino-3-(4-chlorophenyl)propanoate hydrochloride 98%
Supplier:
AMBEED, INC
Description:
Ethyl 5-amino-1-(4-chlorophenyl)-1H-pyrazole-4-carboxylate, Purity: 95%, CAS number: 14678-87-6, Appearance: Light yellow to yellow powder or crystals, Storage: Keep in dark place, Inert atmosphere, 2-8C, Size: 250MG
Catalog Number:
(77748-483)
Supplier:
AMBEED, INC
Description:
(S)-1-(3-Chlorophenyl)propane-1,3-diol ≥97%
Catalog Number:
(76099-472)
Supplier:
Bioss
Description:
C9orf135 (chromosome 9 open reading frame 135) is a 229 amino acid single-pass membrane protein encoded by a gene that maps to human chromosome 9q21.11. 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:
(10670-912)
Supplier:
Bioss
Description:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases, such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD22 (ankyrin repeat domain 22) is a 191 amino acid protein that contains four ANK repeats. Conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, ANKRD22 is encoded by a gene that maps to human chromosome 10. Chromosome 10 encodes nearly 1,200 genes within 135 million bases, making up approximately 4.5% of the human genome. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Catalog Number:
(101911-202)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 056686-5G , MDL Number: MFCD00022116
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 048863-2.5G , MDL Number: MFCD09046144
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 048848-2.5G , MDL Number: MFCD09741165
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 048847-2.5G , MDL Number: MFCD12168024
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 048930-2.5G , MDL Number: MFCD03906866
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 048921-2.5G , MDL Number: MFCD09045205
Supplier:
Matrix Scientific
Description:
MF=C8H5CL MW=136.58 CAS=873-31-4 MDL=MFCD00269951 5G
Supplier:
Matrix Scientific
Description:
MF=C22H14CL2I2N2O2 MW=663.08 CAS=57808-65-8 MDL=MFCD00661151 5G
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