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2-(4-Chlorophenyl)-2,2-difluoroacetic+acid
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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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 is still displayed and you need assistance, please call us at 1-800-932-5000.
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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