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22-(tert-Butoxy)-22-oxodocosanoic+acid
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22-(tert-Butoxy)-22-oxodocosanoic+acid
Supplier:
AMBEED, INC
Description:
Ethyl 2,2-dichloro-3-oxobutanoate 95%
Supplier:
AOB CHEM USA
Description:
5-Iodo-2,2'-bithiophene ≥97%
Catalog Number:
(102846-758)
Supplier:
AMBEED, INC
Description:
4,4'-Dinonyl-2,2'-bithiazole 98+%
Supplier:
Matrix Scientific
Description:
2,2-Dimethyl-2'-methoxypropiophenone ≥97%
Supplier:
Matrix Scientific
Description:
2,2-Dimethyl-4'-methoxybutyrophenone ≥97%
Supplier:
AMBEED, INC
Description:
2,2'-Dinaphthylamine 98%
Clearance
Supplier:
VWR International
Description:
The cleanroom paper is ideal for documentation in critical environments, where very low particle and ESD generation is important.
Supplier:
AMBEED, INC
Description:
[2,2'-Bipyridine]-4-carbaldehyde, Purity: 95%, CAS Number: 146581-82-0, Appearance: Solid, Storage: Inert atmosphere, 2-8 C, Size: 100mg
Supplier:
TCI America
Description:
2,2'-Diaminobiphenyl, Purity: >99.0%(GC)(T), CAS number: 1454-80-4, Molecular Formula: C12H12N2, Molecular Weight: 184.24, Synonyms: [1,1'-Biphenyl]-2,2'-diamine, Form: Crystal - Powder, White - Yellow red, Size: 1G
Supplier:
AOB CHEM USA
Description:
Pyridine, 4-bromo-2-(2,2-difluoroethoxy)- ≥95%
Catalog Number:
(10298-594)
Supplier:
Bioss
Description:
This gene encodes a G-protein beta-subunit-like polypeptide which is a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This protein contains 6 WD repeats and is highly expressed in the heart. The gene maps to the region on chromosome 22q11, which is deleted in DiGeorge syndrome, trisomic in derivative 22 syndrome and tetrasomic in cat-eye syndrome. Therefore, this gene may contribute to the etiology of those disorders. Transcripts from this gene share exons with some transcripts from the C22orf29 gene. [provided by RefSeq, Jul 2008].
Supplier:
AMBEED, INC
Description:
6,6''-Dibromo-2,2':6',2''-terpyridine 98%
Supplier:
AMBEED, INC
Description:
4-Chloro-2,2'-bipyridine 95%
Supplier:
AMBEED, INC
Description:
5-Methyl-2,2'-bipyridine 98%, Ambeed.Inc
Catalog Number:
(10314-160)
Supplier:
Bioss
Description:
C9orf169 (chromosome 9 open reading frame 169) is a 423 amino acid single-pass membrane protein that belongs to the clpA/clpB family and torsin subfamily. The gene encoding C9orf169 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.
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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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