Text Search >
3-[1,1'-Biphenyl]-4-ylacrylic+acid
Print…
You Searched For:
157,843 results were found
3-[1,1'-Biphenyl]-4-ylacrylic+acid
Catalog Number:
(10116-410)
Supplier:
Prosci
Description:
Polyclonal; Host: Goat; Species Reactiviy: Human, Rat; Immunogen: PDK1 antibody was raised against an 11 amino acid synthetic peptide near the internal region of PDK1; Application: ELISA, Western Blot
Supplier:
Matrix Scientific
Description:
MF=C16H18N2 MW=238.34 MDL=MFCD05864686 1G
Catalog Number:
(10483-872)
Supplier:
Bioss
Description:
GLB1L3 is a 653 amino acid protein belonging to the glycosyl hydrolase 35 family. GLB1L3 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q25. 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. 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:
Matrix Scientific
Description:
3-(2-Biphenyl)-1-propene ≥97%
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Biphenyl-4-sulphonyl chloride 97%
Catalog Number:
(77438-616)
Supplier:
Bioss
Description:
Myeov is a 313 amino acid protein that is overexpressed in a variety of cancers and is thought to play a prominent role in tumor transformation and metastasis. The gene encoding Myeov maps to human chromosome 11, which comprises approximately 4% of human genomic DNA and is considered a gene and disease association dense chromosome. MYEOV2 (myeloma overexpressed 2) is a 57 amino acid protein that exists as two alternatively spliced isoforms and belongs to the MYEOV2 family. MYEOV2 is encoded by a gene that maps to human chromosome 2q37.3.
Catalog Number:
(76074-244)
Supplier:
Prosci
Description:
EphA7, polyclonal antibody, Host: Rabbit, Species: Human, Isotype: Ig, Immunogen: KLH conjugated synthetic peptide between 896-925 amino acids from the C-terminal region, Synonyms: EPH-like kinase 11, EK11, hEK11, EPHA7, E
Supplier:
AMBEED, INC
Description:
3-Chloro-4-fluorocinnamic acid 97%
Supplier:
Matrix Scientific
Description:
Methyl-3-biphenyl-4-yl-3-oxopropanoate
Catalog Number:
(89360-214)
Supplier:
Genetex
Description:
EDG7 is a member of the G protein-coupled receptor family, as well as the EDG family of proteins. This protein functions as a cellular receptor for lysophosphatidic acid and mediates lysophosphatidic acid-evoked calcium mobilization. This receptor couples predominantly to G(q/11) alpha proteins.EDG7 has been reported in human prostate, as well as rodent brain, kidney, lung, placenta, prostate, and testis. ESTs have been isolated from a normal prostate library, as well as cancer libraries of the head/neck, ovary, and thyroid.
Supplier:
TCI America
Description:
CAS Number: 627-11-2
MDL Number: MFCD00000646 Molecular Formula: C3H4Cl2O2 Molecular Weight: 142.96 Purity/Analysis Method: >98.0% (T) Form: Clear Liquid Boiling point (°C): 154 Flash Point (°C): 60 Specific Gravity (20/20): 1.38 Storage Temperature: 0-10°C
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:
(76120-282)
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:
(76120-284)
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:
(76120-540)
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.
Inquire for Price
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.
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
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at 1-800-932-5000.
|
|||||||||
List View
