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4-Ethynyl-1,1'-biphenyl
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4-Ethynyl-1,1'-biphenyl
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:
(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:
(10115-668)
Supplier:
Prosci
Description:
Polyclonal antibody BMPR1A Host: Goat Target Species: human immunogen: BMPR1A antibody was raised against an 11 amino acid synthetic peptide near the internal region of BMPR1A. Application: ELISA, WB
Catalog Number:
(10115-664)
Supplier:
Prosci
Description:
Polyclonal antibody BIM Host: Goat Target Species: human immunogen: BIM antibody was raised against an 11 amino acid synthetic peptide near the C-Terminus of BIM. Application: ELISA, WB, IHC
Catalog Number:
(BJ230952-500G)
Supplier:
Honeywell Research Chemicals
Description:
Sodium carbonate monohydrate, ACS Reagent, CAS Number: 5968-11-6, Purity: >/= 99.5%, Linear Formula: Na2CO3 a.H2O, Molar Mass: 124.00 g/mol, Laboratory Chemical, ACS Grade Salt, Size: 500G
Catalog Number:
(10814-636)
Supplier:
Thermo Scientific Chemicals
Description:
CAS No.: 127103-11-1
Molecular Formula: C20H33N5O9 Formula Weight: 487.50 Storage Temperature: -30°C to -10°C Physical Form: Solid Appearance: White to off-white Solubility: Soluble in water at 2mg/ml MDL No.: MFCD00076849
Catalog Number:
(10453-640)
Supplier:
Bioss
Description:
Receptor for interleukin-11. The receptor systems for IL6, LIF, OSM, CNTF, IL11 and CT1 can utilize IL6ST for initiating signal transmission. The IL11/IL11RA/IL6ST complex may be involved in the control of proliferation and/or differentiation of skeletogenic progenitor or other mesenchymal cells.
Supplier:
BeanTown Chemical
Description:
CAS: 57-11-4; EC No: 200-313-4; MDL No: MFCD00002752; RTECS: WI2800000
Solid; Linear Formula: CH3(CH2)16COOH; Molecular Formula: C18H36O2; MW: 284.48
Melting Point: 67-72°; Boiling Point: 361°; Flash point: <gt/>110°C (<gt/>230°F)
Density (g/mL): 0.845
Catalog Number:
(AAJ64202-MB)
Supplier:
Thermo Scientific Chemicals
Description:
AMG-9810, Cas Number: 545395-94-6, Molecular Formula: C21H23NO3, Molecular Weight: 337.41, Appearance: Solid, Synonym: 2E-N-(2,3-Dihydro-1,4-benzodioxin-6-yl)-3-[4-(1,1-dimethylethyl)phenyl]-2-Propenamide, Size: 25mg
Catalog Number:
(89364-772)
Supplier:
Genetex
Description:
Mouse monoclonal [12D7] to MRE11
Catalog Number:
(TCD5102-5G)
Supplier:
TCI America
Description:
4,6-Diacetylresorcinol, Purity: >98.0%(GC)(T), CAS Number: 2161-85-5, Molecular Formula: C10H10O4, Molecular Weight: 194.19, Synonyms: 4,6-Diacetyl-1,3-dihydroxybenzene, 1,1'-(4,6-Dihydroxy-1,3-phenylene)bisethanone, Size: 5G
Catalog Number:
(89321-598)
Supplier:
Genetex
Description:
Purity: Purified by antigen-affinity chromatography. Species Reactivity: Human Tested Applications: ICC/IF, IHC-P, WB Pkg Size: 100 ul
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.
Catalog Number:
(76120-282)
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.
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.
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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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