2-(4-Chlorophenyl)-2,2-difluoroacetic+acid
Catalog Number:
(101822-698)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 026709-500MG , MDL Number: MFCD08544225
Catalog Number:
(76010-916)
Supplier:
Prosci
Description:
This gene is a member of the protocadherin gamma gene cluster, one of three related clusters tandemly linked on chromosome five. These gene clusters have an immunoglobulin-like organization, suggesting that a novel mechanism may be involved in their regulation and expression. The gamma gene cluster includes 22 genes divided into 3 subfamilies. Subfamily A contains 12 genes, subfamily B contains 7 genes and 2 pseudogenes, and the more distantly related subfamily C contains 3 genes. The tandem array of 22 large, variable region exons are followed by a constant region, containing 3 exons shared by all genes in the cluster. Each variable region exon encodes the extracellular region, which includes 6 cadherin ectodomains and a transmembrane region. The constant region exons encode the common cytoplasmic region. These neural cadherin-like cell adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the gamma cluster genes.
Supplier:
AMBEED, INC
Description:
CITCO ≥98%
Supplier:
AMBEED, INC
Description:
2-(4-Chlorophenyl)-3-methyl-1,3-thiazinan-4-one 1,1-dioxide, Purity: 98%, CAS Number: 80-77-3, Appearance: White to Almost white Crystal or Powder, Storage: Sealed in dry, Room Temperature, Size: 1MG
Supplier:
AOB CHEM USA
Description:
2-(5-(Tert-butyl)-2-chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane ≥97%
Supplier:
AMBEED, INC
Description:
(2-Chlorophenyl)(phenyl)methanone, Purity: 98%, CAS Number: 5162-03-8, Appearance: White to Yellow Solid or Semi-solid or liquid or lump, Storage: Sealed in dry, Room Temperature, Size: 1000g
Supplier:
AMBEED, INC
Description:
1-(3-Chlorophenyl)propan-1-one, Purity: 98%, CAS Number: 34841-35-5, Appearance: Form: Crystal - Powder / Colour: White - Slightly pale yellow, Storage: Sealed in dry, Room Temperature, Size: 1000G
Catalog Number:
(101822-668)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 026692-500MG , MDL Number: MFCD09997690
Catalog Number:
(10318-322)
Supplier:
Bioss
Description:
C9orf16 (chromosome 9 open reading frame 16) is an 83 amino acid protein that belongs to the UPF0184 (EST00098) family and is encoded by a gene that maps to human chromosome 9q34.11. 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:
(10318-274)
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:
(101822-712)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 026717-500MG , MDL Number: MFCD09997704
Supplier:
AMBEED, INC
Description:
(2-Amino-5-chlorophenyl)(phenyl)methanone, Purity: 98%, CAS Number: 719-59-5, Appearance: Form: Crystal - Powder, Storage: Keep in dark place, Sealed in dry, Room Temperature, Size: 100G
Catalog Number:
(76803-462)
Supplier:
AMBEED, INC
Description:
Methyl 3-(2-Chlorophenyl)-3-oxopropionate, Purity: 95%, CAS Number: 205985-98-4, Appearance: Pale-yellow to Yellow-brown Liquid, Storage: Sealed in dry, 2-8C, Size: 5G
Catalog Number:
(101931-464)
Supplier:
Matrix Scientific
Description:
MF=C15H12Cln5 MW=297.75 MDL=MFCD05843860 ,500Mg
Catalog Number:
(10298-602)
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].
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