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(2S,2'S)-2,2'-(Hexadecanedioylbis(azanediyl))dipentanedioic+acid
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(2S,2'S)-2,2'-(Hexadecanedioylbis(azanediyl))dipentanedioic+acid
Catalog Number:
(102891-696)
Catalog Number:
(10318-316)
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:
(10314-324)
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:
(10314-130)
Supplier:
Bioss
Description:
C9orf142 (chromosome 9 open reading frame 142) is a 204 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf142 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:
(77748-867)
Supplier:
AMBEED, INC
Description:
(2S,3S)-2-Amino-3-methyl-N-(2-morpholinoethyl)pentanamide ≥97%
Catalog Number:
(102891-340)
Catalog Number:
(10314-108)
Supplier:
Bioss
Description:
C9orf140 (chromosome 9 open reading frame 140), also known as TS/MDEP (tumor specificity and mitosis phase-dependent expression protein) or p42.3, is a 394 amino acid nuclear and cytoplasmic protein encoded by a gene that 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:
(76822-292)
Supplier:
AMBEED, INC
Description:
(1S,2S)-2-(Benzylamino)cyclohexanol, Purity: 97%, CAS Number: 322407-34-1, Appearance: White to off-white solid, Storage: Keep in dark place, Inert atmosphere, 2-8C, Size: 5G
Catalog Number:
(77623-016)
Supplier:
AMBEED, INC
Description:
(2S)-2-Amino-2-cyclopropylethan-1-ol hydrochloride ≥95%
Supplier:
AMBEED, INC
Description:
(2S,4R)-tert-Butyl 4-hydroxy-2-methylpyrrolidine-1-carboxylate, Purity: 95%, CAS Number: 114676-61-8, Appearance: White to Yellow Solid, Storage: Sealed in dry, 2-8C, Size: 5G
Supplier:
AMBEED, INC
Description:
(1S,2S,4R)-1-Methyl-2,4-di(prop-1-en-2-yl)-1-vinylcyclohexane ≥98%
Supplier:
AMBEED, INC
Description:
(2S,4S)-1-Benzyl 2-methyl 4-aminopyrrolidine-1,2-dicarboxylate hydrochloride, Purity: 95%, CAS number: 1515919-15-9, Appearance: Solid, Storage: Inert atmosphere, 2-8C, Size: 25G
Supplier:
TCI America
Description:
CAS Number: 19132-06-0
MDL Number: MFCD00063648 Molecular Formula: C4H10O2 Molecular Weight: 90.12 Purity/Analysis Method: >97.0% (GC) Form: Clear Liquid Boiling point (°C): 182 Flash Point (°C): 85 Freezing point (°C): 17 Specific Gravity (20/20): 0.99 Specific rotation [a]20/D: 13.5 deg (neat)
Supplier:
AMBEED, INC
Description:
tert-Butyl ((1S,2S)-2-hydroxycyclopentyl)carbamate, Purity: 99%, CAS Number: 145106-43-0, Appearance: Solid or liquid, Storage: Keep in dark place, Sealed in dry, 2-8C, Size: 25G
Supplier:
AMBEED, INC
Description:
(1S,2S)-2-(Diphenylphosphino)cyclohexanamine, Purity: 98%, CAS number: 452304-63-1, Appearance: Form: solid, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 1G
Supplier:
TCI America
Description:
CAS Number: 29841-69-8
MDL Number: MFCD00082751 Molecular Formula: C14H16N2 Molecular Weight: 212.30 Purity/Analysis Method: >98.0% (GC,T) Form: Crystal Melting point (°C): 83 Specific rotation [a]20/D: -103 deg (C=1, EtOH)
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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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