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2,2-Difluoro-4-pentenoic+acid
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2,2-Difluoro-4-pentenoic+acid
Supplier:
AOB CHEM USA
Description:
1-Ethoxy-2,3-difluoro-4-iodobenzene ≥97%
Supplier:
AOB CHEM USA
Description:
Methyl 2,5-difluoro-4-hydroxybenzoate ≥97%
Catalog Number:
(76107-830)
Supplier:
Bioss
Description:
C9orf153 is a 101 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf153 maps to human chromosome 9q21.33. 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.
Catalog Number:
(76107-828)
Supplier:
Bioss
Description:
C9orf153 is a 101 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf153 maps to human chromosome 9q21.33. 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:
4-Chloro-2,6-difluoro-3-hydroxybenzaldehyde ≥97%
Supplier:
AOB CHEM USA
Description:
(2,5-Difluoro-4-methylsulfanylphenyl)methanol ≥95%
Supplier:
AMBEED, INC
Description:
5,7-Difluoro-1-indanone 95%
Supplier:
AOB CHEM USA
Description:
4,5-Difluoro-2-hydroxybenzonitrile ≥97%
Supplier:
AMBEED, INC
Description:
2,6-Difluoro-3-nitrobenzonitrile 98%
Supplier:
Matrix Scientific
Description:
MF=C8H6F2O MW=156.13 Cas=261763-34-2 MDL=MFCD01631333 1G
Supplier:
Thermo Scientific Chemicals
Description:
N-Boc-3,5-difluoro-L-phenylalanine, 95%
Catalog Number:
(10250-122)
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:
2,6-Difluoro-4-isobutoxybenzaldehyde ≥97%
Supplier:
AOB CHEM USA
Description:
3,4-Difluoro-2-methoxybenzamide ≥97%
Supplier:
AMBEED, INC
Description:
2,4-Difluoro-5-methoxybenzaldehyde, Purity: 97%, CAS Number: 177034-25-2, Appearance: Solid, Storage: Inert atmosphere, 2-8 C, Size: 5g
Catalog Number:
(76011-642)
Supplier:
Prosci
Description:
The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities and are involved in a variety of biological processes including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. The mouse homolog of this gene was found to be preferentially expressed in the inner root sheath of the hair follicle, which suggested a role in hair development. [provided by RefSeq].
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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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