ENCAB708RYV

Antibody against Homo sapiens NCOA1

Homo sapiens
K562
characterized to standards
Homo sapiens
GM12878, MCF-7, HepG2
partially characterized
Status
released
Source (vendor)
Bethyl Labs
Product ID
A300-343A
Lot ID
2
Characterized targets
NCOA1 (Homo sapiens)
Host
rabbit
Clonality
polyclonal
Purification
affinity
Aliases
michael-snyder:AS-1370
External resources

Characterizations

NCOA1 (Homo sapiens)
K562
Method: immunoprecipitation
Attachment from submitter
compliant
Caption
Immunoprecipitation was performed on nuclear extracts from the cell line: K562, using the antibody A300-343A. The blot shows western blot analysis of input, flowthrough, immunoprecipitate and mock immunoprecipitate using IgG. Expected Molecular Weight: 157 KD
Submitted by
Denis Salins
Lab
Michael Snyder, Stanford
NCOA1 (Homo sapiens)
GM12878
Method: immunoprecipitation
Attachment from submitter
Caption
Immunoprecipitation was performed on nuclear extracts from the cell line: GM12878 using the antibody A300-343A. The image shows western blot analysis of input, flowthrough, immunoprecipitate, and mock immunoprecipitate using IgG. Target molecular weight: 156.757.
Submitted by
Nathaniel Watson
Lab
Michael Snyder, Stanford
NCOA1 (Homo sapiens)
MCF-7
Method: immunoprecipitation
Attachment from submitter
Caption
Immunoprecipitation was performed on nuclear extracts from the cell line: MCF-7 using the antibody A300-343A. The image shows western blot analysis of input, flowthrough, immunoprecipitate, and mock immunoprecipitate using IgG. Target molecular weight: 156.757.
Submitted by
Nathaniel Watson
Lab
Michael Snyder, Stanford
NCOA1 (Homo sapiens)
Method: immunoprecipitation followed by mass spectrometry
compliant
Caption
IP followed by mass spectrometry. Briefly, protein was immunoprecipitated from K562 nuclear cell lysates using the antibody A300-343A, and the IP fraction was loaded on a 10% polyacrylamide gel (NuPAGEBis-Tris Gel) and separated with an Invitrogen NuPAGE electrophoresis system. The gel was stained by ColloidialCoomassie G-250 stain, gel fragments corresponding to the bands indicated were excised. Then proteins were trypsinized using the in-gel digestion method. Digested proteins were analyzed on an Orbitrap Elite mass spectrometer (Thermo Scientific) by the nanoLC-ESI-MS/MS technique. Peptides were identified by the SEQUEST algorithm and filtered with a high confidence threshold (Peptide false discovery rate < 1%, 2 unique peptides per protein minimum, mass error < 10 ppm).
Submitter comment
NCOA1 has interaction with WDHD1 http://thebiogrid.org/114200/summary/homo-sapiens/ncoa1.html
Submitted by
Nathaniel Watson
Lab
Michael Snyder, Stanford
NCOA1 (Homo sapiens)
K562
Method: immunoprecipitation
Attachment from submitter
compliant
Caption
Immunoprecipitation was performed on nuclear extracts from the cell line K562 using the antibody A300-343A. Lane 1: input nuclear lysate. Lane 2: material immunoprecipitated with antibody. Lane 3: material immunoprecipitated using control IgG. Marked bands were excised from gel and subjected to analysis by mass spectrometry. Target molecular weight: 156.757.
Submitted by
Nathaniel Watson
Lab
Michael Snyder, Stanford
NCOA1 (Homo sapiens)
HepG2
Method: immunoprecipitation
Attachment from submitter
Caption
Immunoprecipitation was performed on nuclear extracts from the cell line: HepG2 using the antibody A300-343A. The image shows western blot analysis of input, flowthrough, immunoprecipitate, and mock immunoprecipitate using IgG. Target molecular weight: 156.757.
Submitted by
Nathaniel Watson
Lab
Michael Snyder, Stanford