(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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