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2,2-Difluoro-4-pentenoic+acid
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2,2-Difluoro-4-pentenoic+acid
Supplier:
Matrix Scientific
Description:
2,5-DIFLUORO-4-IODOPYRIDINE MF=C5H2F2IN MW=240.98 CAS=1017793-20-2 MDL=MFCD11040606
Supplier:
AOB CHEM USA
Description:
3,6-Difluoro-2-iodophenol ≥97%
Catalog Number:
(10237-618)
Supplier:
Bioss
Description:
Epithelial membrane protein-1 (EMP-1) is a four pass transmembrane protein consisting of 160 amino acids. It is a member of a small family of epithelial membrane proteins. EMP-1 is very similar in structure to its close relative, Peripheral Myelin Protein 22 (PMP22). It is most predominantly expressed in tissues of the gastrointestinal tract but has also been found to be a junctional protein in the liver expressed along the intercellular border. EMP-1 directly interacts with the C-terminus of the P2X7 receptor and may be involved in membrane blebbing. EMP-1 may also be an important regulator in cell communication, signaling, and adhesion. When EMP-1 is overexpressed, cell proliferation is inhibited, S phase is arrested and G1 phase is prolonged in esophogeal cancer cells. EMP-1 may play a role in tumorigenesis and has been identified as a biomarker for gefitinib treatment resistance for patients with lung cancer.
Supplier:
AOB CHEM USA
Description:
1-Bromo-2,4-difluoro-3-methoxybenzene 97 Research
Supplier:
AOB CHEM USA
Description:
2,4-Difluoro-3-iodobenzaldehyde ≥97%
Catalog Number:
(10318-286)
Supplier:
Bioss
Description:
C9orf139 (chromosome 9 open reading frame 139) is a 190 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:
(10318-336)
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:
(10314-686)
Supplier:
Bioss
Description:
C9orf79 is a 1,445 amino acid single-pass membrane protein that belongs to the FAM75 family. The gene encoding C9orf79 maps to human chromosome 9, which consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered 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:
(PI21331)
Supplier:
Invitrogen
Description:
Thermo Scientific EZ-Link Sulfo-NHS-SS-Biotin is a water-soluble, NHS-ester biotinylation reagent whose spacer arm includes a cleavable disulfide bond for reversible labeling of proteins and cell surface primary amines.
Supplier:
AOB CHEM USA
Description:
2,5-Difluoro-3-methylbenzaldehyde ≥97%
Supplier:
BeanTown Chemical
Description:
CAS: 134412-18-3; MDL No: MFCD12828121
Powder; Molecular Formula: C20H22F2; MW: 300.39
Melting Point: 68-69°
Supplier:
AOB CHEM USA
Description:
2,6-Difluoro-3-(methylthio)benzaldehyde ≥95%
Supplier:
AOB CHEM USA
Description:
2-Ethoxy-1,3-difluoro-5-iodobenzene ≥97%
Supplier:
AOB CHEM USA
Description:
1-Bromo-2,3-difluoro-4-isopropoxybenzene ≥97%
Supplier:
AOB CHEM USA
Description:
1-(3,5-Difluoro-4-iodophenyl)ethanone ≥97%
Supplier:
AOB CHEM USA
Description:
1-(Benzyloxy)-2,3-difluoro-5-iodobenzene ≥97%
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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.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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