Pyrazine-2,6-diamine+hydrochloride
Catalog Number:
(10270-108)
Supplier:
Bioss
Description:
TMEM132A is a 560 amino acid protein encoded by a gene mapping to human chromosome 11. With approximately 135 million base pairs and 1,400 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:
WORLD PRECISION INSTRUMENTS LLC
Description:
Scalpels are used for removing tissue and making initial incisions. Typically, a scalpel is comprised of a blade and a handle. Scalpels are purchase based on the blade number which indicates its shape. The most popular blades are the #10, #11 and #15.
Supplier:
Matrix Scientific
Description:
MF=C18H20N2O MW=280.37 CAS=133099-11-3 MDL=MFCD09263622 1G
Supplier:
AMBEED, INC
Description:
4-[(Diethylcarbamoyl)amino]benzeneboronic acid, pinacol ester 98%
Catalog Number:
(10270-096)
Supplier:
Bioss
Description:
TMEM132A is a 560 amino acid protein encoded by a gene mapping to human chromosome 11. With approximately 135 million base pairs and 1,400 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:
(S)-1-Benzyl 3-ethyl piperidine-1,3-dicarboxylate, Purity: 97%, CAS Number: 174699-11-7, Appearance: Colorless to Yellow Liquid, Storage: Sealed in dry, Room Temperature, Size: 5G
Supplier:
AMBEED, INC
Description:
2-(4-Chlorophenoxy)aniline, Purity: 98%, CAS Number: 2770-11-8, Appearance: Form: liquid/Colour: Colorless - yellow - brown, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 1g
Supplier:
AMBEED, INC
Description:
Chaetocin 99+%
Catalog Number:
(101418-894)
Supplier:
Strem Chemicals Inc
Description:
BINAP
Supplier:
AMBEED, INC
Description:
3-Bromo-1,1-dimethoxypropane, Purity: 97%, CAS Number: 36255-44-4, Appearance: Form: liquid/Colour: Colorless - yellow - Brown, Storage: Inert atmosphere, 2-8 C, Size: 1g
Supplier:
AMBEED, INC
Description:
trans,trans-4'-n-Propylbicyclohexyl-4-carboxylic acid 97%
Supplier:
AMBEED, INC
Description:
2,3,6,7,10,11-Hexamethoxytriphenylene 97%
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 041334-1G , MDL Number: MFCD06410966
Catalog Number:
(75843-390)
Supplier:
BIOGEMS INTERNATIONAL INC.
Description:
The MPC-11 monoclonal antibody is expressed by a cell line adapted from the Merwin Plasmacytoma-11, and has unknown specificity. The MPC-11 line was obtained by intraperitoneal implantation into a BALB/c Mouseof a Millipore diffusion chamber and is used as an Isotype Control for MouseIgG2b antibodies.BG Violet 450 conjugate is an alternative to the Pacific Blue, eFluor 450, or BD Horizon V450 dyes. It is excited by the violet (405 nm) laser, with a peak emission of 450nm.
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