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4-Ethynyl-1,1\\\\\\\\\\\\\\\'-biphenyl
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4-Ethynyl-1,1\\\\\\\\\\\\\\\'-biphenyl
Catalog Number:
(10761-000)
Supplier:
Biolegend
Description:
Brilliant Violet 421™ anti-mouse IgD [11-26c.2a]; Isotype: Rat IgG2a, κ; Reactivity: Mouse; Apps: FC; Size: 50 μg
Supplier:
AMBEED, INC
Description:
(3R,4S)-4-Aminotetrahydro-2H-pyran-3-ol hydrochloride, Purity: 98%, CAS Number: 1096594-11-4, Appearance: White to yellow powder or crystals, Storage: Inert atmosphere, Room Temperature, Size: 100mg
Catalog Number:
(76990-298)
Supplier:
AMBEED, INC
Description:
Methyl 2-amino-5-fluoro-3-nitrobenzoate, Purity: 97%, CAS number: 328547-11-1, Appearance: Solid, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 250MG
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Ethylene diacrylate 95% stabilized
Supplier:
AOB CHEM USA
Description:
4-Phenoxy-2-methoxyphenylboronic acid ≥97%
Catalog Number:
(77119-800)
Supplier:
Prosci
Description:
Human Recombinant TREM2 Protein (from HEK293 cells)
Supplier:
AMBEED, INC
Description:
3-(1,1,1,5,5,5-Hexamethyl-3-((trimethylsilyl)oxy)trisiloxan-3-yl)propyl methacrylate, Purity: 95% (stabilized with MEHQ), CAS Number: 17096-07-0, Appearance: Form: liquid/Colour: Colorless - Red-brown, Storage: Inert atmosphere, Room Temperature, Size: 500g
Supplier:
Corning
Description:
Axygen® Gel Cutting Tips are designed to remove bands from agarose gel.
Supplier:
Bachem Americas
Description:
25mg CAS: 51165-09-4 C41H60N10O9S FW: 869.06 . Substance P
Catalog Number:
(76120-292)
Supplier:
Bioss
Description:
C11orf71, also known as FLJ20010, is a 123 amino acid protein that exists as two alternatively spliced isoforms and is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
Catalog Number:
(76120-284)
Supplier:
Bioss
Description:
C11orf57, also known as FLJ10726, is a 292 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
Supplier:
Strem Chemicals Inc
Description:
CAS #: 598-30-1. Size: 0.25mole.
Supplier:
TCI America
Description:
3-(4-Methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)aniline, Purity: >98.0%(GC)(T), CAS Number: 641571-11-1, MF: C11H10F3N3, Molecular Weight: 241.22, Synonyms: 1-[3-Amino-5-(trifluoromethyl)phenyl]-4-methylimidazole, Size: 5G
Catalog Number:
(76120-540)
Supplier:
Bioss
Description:
C11orf74, also known as FLJ38678, is a 123 amino acid protein that exists as two alternatively spliced isoforms and is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1400 genes, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
Supplier:
AMBEED, INC
Description:
5-Chloro-2-cyano-3-nitropyridine, Purity: 98%, CAS Number: 181123-11-5, Appearance: White to yellow powder or crystals, Storage: Inert atmosphere, Room Temperature, Size: 10g
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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.
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