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3-[1,1\\\\\\\\\\\\\\\'-Biphenyl]-4-ylacrylic+acid
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3-[1,1\\\\\\\\\\\\\\\'-Biphenyl]-4-ylacrylic+acid
Catalog Number:
(10113-070)
Supplier:
Prosci
Description:
Polyclonal, Host: Goat, Immunogen: Forkhead Box I2 antibody was raised against an 11 amino acid synthetic peptide near the C-Terminus of Forkhead Box I2, Application: ELISA
Supplier:
Enzo Life Sciences
Description:
Recommended Applications: IP, WB
Species reactivity:
Supplier:
Spectrum Chemicals
Description:
Bromocresol Purple is a pH indicator that is typically prepared as a 0.04% solution. It is used to measure albumin in medical laboratories and is added to acid stop baths used in photographic film processing to indicate when the solution is no longer acidic and needs to be replaced
Catalog Number:
(76107-960)
Supplier:
Bioss
Description:
Zinc is an essential cofactor that is involved in cell growth and development, as well as in protein, nucleic acid and lipid metabolism. The transport of zinc across the cell membrane is crucial for correct enzyme and overall cell function. SLC39A11 (solute carrier family 39 (metal ion transporter), member 11), also known as ZIP11 (Zrt- and Irt-like protein 11), is a 342 amino acid multi-pass membrane protein belonging to the ZIP transporter family. Expressed as multiple alternatively spliced isoforms, SLC39A11 acts as a zinc-influx transporter and is encoded by a gene located on human chromosome 17, which comprises over 2.5% of the human genome and encodes over 1,200 genes, some of which are involved in tumor suppression and in the pathogenesis of Li-Fraumeni syndrome, early onset breast cancer and a predisposition to cancers of the ovary, colon, prostate gland and fallopian tubes.
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:
(10114-974)
Supplier:
Prosci
Description:
Polyclonal, Host: Goat; Target Species: Human; Immunogen: PRKAA2 antibody was raised against an 11 amino acid synthetic peptide near the internal region of PRKAA2; Applications: ELISA,Western blotting
Catalog Number:
(10114-948)
Supplier:
Prosci
Description:
Polyclonal, Host: Goat; Target Species: Human; Immunogen: NDUFS7 antibody was raised against an 11 amino acid synthetic peptide near the internal region of NDUFS7; Applications: ELISA,Western blotting
Catalog Number:
(10113-422)
Supplier:
Prosci
Description:
Polyclonal, Host: Goat, Species Reactivity: Human, Immunogen: TBP antibody was raised against a 11 amino acid synthetic peptide near the N-Terminus of TBP (isoform1), Tested Applications: ELISA, WB
Catalog Number:
(10114-570)
Supplier:
Prosci
Description:
Polyclonal, Host: Goat; Target Species: Human; Immunogen: BOD1 antibody was raised against an 11 amino acid synthetic peptide near the internal region of BOD1; Applications: ELISA,Western blotting
Catalog Number:
(10116-948)
Supplier:
Prosci
Description:
Polyclonal; Host: Goat; Species Reactiviy: Human; Immunogen: NO66 antibody was raised against an 11 amino acid synthetic peptide near the internal region of NO66; Application: ELISA, Western Blot
Catalog Number:
(101823-648)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 027170-500MG , MDL Number: MFCD09055221
Supplier:
Thermo Scientific Chemicals
Description:
MDL: MFCD00002683
Beilstein Registry No.: 605438
Soluble in water, alcohols, benzene, chloroform, ether
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:
(10114-704)
Supplier:
Prosci
Description:
Polyclonal, Host: Goat; Immunogen: LY6E antibody was raised against an 11 amino acid synthetic peptide near the internal region of LY6E (mouse); Applications: ELISA,Western blotting
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:
(10113-612)
Supplier:
Prosci
Description:
Polyclonal, Host: Goat, Species Reactivity: Human, Immunogen: HLA-DQA2 antibody was raised against an 11 amino acid synthetic peptide near the C-Terminus of HLA-DQA2, Tested Applications: ELISA, WB
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 is still displayed and you need assistance, please call us at 1-800-932-5000.
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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