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2,2-Difluoro-4-pentenoic+acid


156,555  results were found

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Supplier:  Bioss
Description:   C9orf25 (chromosome 9 open reading frame 25) is a 185 amino acid protein that exists as seven alternatively spliced isoforms that are encoded by a gene located on human chromosome 9. 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:  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:  AOB CHEM USA
Description:   3,5-Difluoro-4-iodo-4'-methyl-1,1'-biphenyl ≥95%
Supplier:  AOB CHEM USA
Description:   2,6-Difluoro-4-isopropyloxybenzyl alcohol ≥95%
Supplier:  APOLLO SCIENTIFIC
Description:   Ethyl 2-bromo-4,4-difluoro-3-oxobutanoate, Technical Grade
Supplier:  Bioss
Description:   C9orf5 (chromosome 9 open reading frame 5), also known as CG2, is a 911 amino acid multi-pass membrane protein that is widely expressed and exists as four alternatively spliced isoforms. The gene encoding C9orf5 maps to human chromosome 9, which consists of about 145 million bases, represents 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.
Supplier:  AMBEED, INC
Description:   3,4-Difluoro-4'-((trans,trans)-4'-propyl-[1,1'-bi(cyclohexan)]-4-yl)-1,1'-biphenyl, Purity: 98+%, CAS Number: 119990-81-7, Appearance: Solid, Storage: Sealed in dry, Room Temperature, Size: 5G
Supplier:  AOB CHEM USA
Description:   Ethyl 2,3-difluoro-5-methoxy-4-methylbenzoate ≥97%
Supplier:  AMBEED, INC
Description:   Rel-(1r,1'r,4R,4'R)-4-(difluoro(3,4,5-trifluorophenoxy)methyl)-4'-ethyl-1,1'-bi(cyclohexane) ≥98%
New Product
Supplier:  Matrix Scientific
MSDS SDS
Catalog Number: (76072-434)

Supplier:  Prosci
Description:   For WB starting dilution is: 1:1000 For IHC-P starting dilution is: 1:50~100 For FACS starting dilution is: 1:10~50

Supplier:  Matrix Scientific
Description:   Matrix Scientific Part Number: 064044-1G , MDL Number: MFCD12546949

Supplier:  Bioss
Description:   Protocadherins are a large family of cadherin-like cell adhesion proteins that are involved in the establishment and maintenance of neuronal connections in the brain. There are three protocadherin gene clusters designated alpha, beta and gamma, all of which contain multiple tandemly arranged genes. The protocadherein gamma cluster consists of three subfamilies (A, B and C). As a member of the gamma subfamily B, PCDHGB1 (Protocadherin gamma B1) is a 927 amino acid protein that is one of 22 proteins encoded by the protocadherin gamma cluster. Typical of gamma protocadherins, PCDHGB1 contains six cadherin motifs and is a type I transmembrane receptor expressed in the central nervous system. With localization to synapses, members of the gamma cluster of protocadherins are essential for neuronal survival. There are two isoforms of PCDHGB1 that are produced as a result of alternative splicing events.
Supplier:  AOB CHEM USA
Description:   (2,4'-Difluoro-5-methoxy-[1,1'-biphenyl]-3-yl)(methyl)sulfane ≥97%
Supplier:  AOB CHEM USA
Description:   2-Chloro-1,3-difluoro-4-(methoxymethoxy)benzene ≥95%
Supplier:  AOB CHEM USA
Description:   Ethyl 5-bromo-2,3-difluoro-4-methylbenzoate ≥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 call 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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