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4-(Pyrimidin-5-yl)benzoic+acid
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4-(Pyrimidin-5-yl)benzoic+acid
Catalog Number:
(10479-426)
Supplier:
Bioss
Description:
FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which 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:
(10112-278)
Supplier:
Prosci
Description:
Polyclonal, Host: Goat, Species: Human, Immunogen: ABHD4 antibody was raised against an 11 amino acid synthetic peptide near the internal region of ABHD4 (aa 177 to 187), Application: ELISA, WB
Catalog Number:
(76121-102)
Supplier:
Bioss
Description:
C11orf16 is a 404 amino acid protein that 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:
(10265-736)
Supplier:
Bioss
Description:
MPPED2 (Metallophosphoesterase domain-containing protein 2), also known as C11orf8, FAM1B or 239FB, is a 294 amino acid protein. Expressed primarily in fetal brain tissue, MPPED2 is encoded by a gene that maps to 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 stranded 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, while 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:
(10112-818)
Supplier:
Prosci
Description:
Polyclonal, Host: Goat, Species: Human, Immunogen: P2RY1 antibody was raised against an 11 amino acid synthetic peptide near the internal region of P2RY1 (aa 247-257), Application: ELISA
Catalog Number:
(TS13189-0250)
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Pyridine-3,4-dicarboxylic acid 97%
Catalog Number:
(10116-736)
Supplier:
Prosci
Description:
Polyclonal; Host: Goat; Species Reactiviy: Human; Immunogen: SLC9A3R2 antibody was raised against an 11 amino acid synthetic peptide near the internal region of SLC9A3R2; Application: ELISA, Western Blot, IHC
Catalog Number:
(10116-950)
Supplier:
Prosci
Description:
Polyclonal; Host: Goat; Species Reactiviy: Human; Immunogen: CADM4 antibody was raised against an 11 amino acid synthetic peptide near the internal region of CADM4; Application: ELISA, Western Blot, IHC
Catalog Number:
(10116-600)
Supplier:
Prosci
Description:
Polyclonal; Host: Goat; Species Reactiviy: Human; Immunogen: Rhophilin 2 antibody was raised against an 11 amino acid synthetic peptide near the internal region of Rhophilin 2; Application: ELISA, IHC
Supplier:
AMBEED, INC
Description:
3-Methoxy-5-(methoxycarbonyl)phenylboronic acid 98+%, Ambeed.Inc
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 009244-25G , MDL Number: MFCD04038373
Catalog Number:
(IC15255405)
Supplier:
MP Biomedicals
Description:
Phenol Red Sodium Salt is used as a pH indicator, it is used widely in culture media to identify changes from neutral to acidic pH values.
Catalog Number:
(10112-766)
Supplier:
Prosci
Description:
Polyclonal, Host: Goat, Species: Human, Immunogen: OCT4 antibody was raised against an 11 amino acid synthetic peptide near the C-Terminus of 41186, Application: ELISA, WB
Catalog Number:
(10115-494)
Supplier:
Prosci
Description:
Polyclonal antibody PIP Host: Goat Target Species: human immunogen: PIP antibody was raised against an 11 amino acid synthetic peptide near the internal region of PIP. Application: ELISA, WB, IHC
Catalog Number:
(10113-202)
Supplier:
Prosci
Description:
Polyclonal, Host: Goat, Species Reactivity: Human, Immunogen: AIF1 antibody was raised against an 11 amino acid synthetic peptide near the C-Terminus of AIF1, Tested Applications: ELISA, WB, IHC
Catalog Number:
(10113-262)
Supplier:
Prosci
Description:
Polyclonal, Host: Goat, Species Reactivity: Mouse, Immunogen: COL4A3BP antibody was raised against an 11 amino acid synthetic peptide near the internal region of COL4A3BP, Tested Applications: ELISA, WB
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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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