2-(4-Chlorophenyl)-2,2-difluoroacetic+acid
Supplier:
AMBEED, INC
Description:
1-((4-Chlorophenyl)thio)propan-2-one, Purity: 98%, CAS Number: 25784-83-2, Appearance: Form: solid, Storage: Sealed in dry, Room Temperature, Size: 1g
Catalog Number:
(EM1.02498.0025)
Supplier:
Matrix Scientific
Description:
MF=C15H10BRCLN2O MW=349.62 CAS=51753-57-2 MDL=MFCD00423674 1G
Supplier:
AMBEED, INC
Description:
1-(2-Amino-5-chlorophenyl)-2,2,2-trifluoroethanone hydrochloride, Purity: 97%, CAS Number: 173676-59-0, Appearance: White to yellow powder or crystals, Storage: Inert atmosphere, Room Temperature, Size: 100mg
Catalog Number:
(77692-647)
Supplier:
LGC STANDARDS
Description:
(2-Chlorophenyl)(1-hydroxycyclopentyl)methanone, Mikromol, LGC Standards
Supplier:
AMBEED, INC
Description:
Clofazimine 98%
Supplier:
Thermo Scientific Chemicals
Description:
MDL: MFCD00013643
Beilstein Registry No.: 2041509
Catalog Number:
(10314-328)
Supplier:
Bioss
Description:
C9orf23 (chromosome 9 open reading frame 23) is a 163 amino acid protein that belongs to the histone-like Alba family and is encoded by a gene that maps to human chromosome 9p13.3. 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:
(10318-320)
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:
(10314-158)
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.
Catalog Number:
(76010-792)
Supplier:
Prosci
Description:
The protein encoded by this gene is a type I transmembrane AMPA receptor regulatory protein (TARP). TARPs regulate both trafficking and channel gating of the AMPA receptors. This gene is part of a functionally diverse eight-member protein subfamily of the PMP-22/EMP/MP20 family and is located in a cluster with two family members, a type II TARP and a calcium channel gamma subunit. The mRNA for this gene is believed to initiate translation from a non-AUG (CUG) start codon.
Supplier:
AMBEED, INC
Description:
I-BET762 98+%
Catalog Number:
(101835-212)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 033203-500MG , MDL Number: MFCD11506469
Supplier:
AMBEED, INC
Description:
AZD-5363 98%
Supplier:
AMBEED, INC
Description:
Clemastine fumarate 98%
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