AGGF1 polyclonal antibody
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More Files
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Western Blot (Transfected lysate)
Human AGGF1 detected in HT1080 non-transfected cell lysate (NTC) and HT1080 transfected cell lysate (TC) using AGGF1 polyclonal antibody (Cat # PAB12494).
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Specification
Product Description
Rabbit polyclonal antibody raised against synthetic peptide of AGGF1.
Immunogen
A synthetic peptide corresponding to amino acids 500-600 of human AGGF1.
Host
Rabbit
Reactivity
Human
Specificity
This antibody is specific to human VG5Q.
Form
Liquid
Quality Control Testing
Antibody Reactive Against Synthetic Peptide.
Recommend Usage
Immunohistochemistry (1:250)
Western Blot (1:500)
The optimal working dilution should be determined by the end user.Storage Buffer
In antiserum
Storage Instruction
Store at 4°C for short term. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing. -
Applications
Western Blot (Transfected lysate)
Human AGGF1 detected in HT1080 non-transfected cell lysate (NTC) and HT1080 transfected cell lysate (TC) using AGGF1 polyclonal antibody (Cat # PAB12494).Immunohistochemistry
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Gene Info — AGGF1
Entrez GeneID
55109Protein Accession#
Q8N302Gene Name
AGGF1
Gene Alias
FLJ10283, GPATC7, GPATCH7, HSU84971, HUS84971, VG5Q
Gene Description
angiogenic factor with G patch and FHA domains 1
Gene Ontology
HyperlinkGene Summary
The AGGF1 gene encodes a potent angiogenic factor that contains a forkhead-associated domain and a G-patch domain (Tian et al., 2004 [PubMed 14961121]).[supplied by OMIM
Other Designations
angiogenic factor VG5Q|vasculogenesis gene on 5q
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Interactome
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Disease
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Publication Reference
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Identification of an angiogenic factor that when mutated causes susceptibility to Klippel-Trenaunay syndrome.
Tian XL, Kadaba R, You SA, Liu M, Timur AA, Yang L, Chen Q, Szafranski P, Rao S, Wu L, Housman DE, DiCorleto PE, Driscoll DJ, Borrow J, Wang Q.
Nature 2004 Feb; 427(6975):640.
Application：C-ELISA, IS, WB-Ti, IP, Human, Mouse, HMVECs, HUVECs, Kidney.
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Identification of an angiogenic factor that when mutated causes susceptibility to Klippel-Trenaunay syndrome.
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