GABPA Monoclonal antibody, PBS Only
GABPA Monoclonal Antibody for WB, Indirect ELISA
Host / Isotype
Mouse / IgG2a
Reactivity
Human, Mouse, Rat
Applications
WB, Indirect ELISA
Conjugate
Unconjugated
CloneNo.
2A7E3
验证数据展示
Planning an IHC experiment? We recommend our IHCeasy GABPA Ready-To-Use IHC Kit. GABPA primary antibody included.
产品信息
68645-1-PBS targets GABPA in WB, Indirect ELISA applications and shows reactivity with Human, Mouse, Rat samples.
Tested Applications | WB, Indirect ELISA Application Description |
Tested Reactivity | Human, Mouse, Rat |
Immunogen | GABPA fusion protein Ag33705 种属同源性预测 |
Host / Isotype | Mouse / IgG2a |
Class | Monoclonal |
Type | Antibody |
Full Name | GA binding protein transcription factor, alpha subunit 60kDa |
Synonyms | E4TF1 60, E4TF1A, GA binding protein alpha chain, GABP subunit alpha, GABPA, NFT2, Transcription factor E4TF1 60 |
Calculated Molecular Weight | 454 aa, 51 kDa |
Observed Molecular Weight | 56-60 kDa |
GenBank Accession Number | BC035031 |
Gene Symbol | GABPA |
Gene ID (NCBI) | 2551 |
Conjugate | Unconjugated |
Form | Liquid |
Purification Method | Protein A purification |
UNIPROT ID | Q06546 |
Storage Buffer | PBS Only |
Storage Conditions | Store at -80°C. The product is shipped with ice packs. Upon receipt, store it immediately at -80°C |
背景介绍
GA-binding protein alpha chain (GABP alpha subunit, GABPA, nuclear respiratory factor 2 subunit alpha, transcription factor E4TF1-60) is one of three GA-binding protein transcription factor subunits which functions as a DNA-binding subunit.GABPA is a member of Ets family, binds to the Yap promoter and activates YAP transcription(23684612). Since this subunit shares identity with a subunit encoding the nuclear respiratory factor 2 gene, it is likely involved in activation of cytochrome oxidase expression and nuclear control of mitochondrial function. This subunit also shares identity with a subunit constituting the transcription factor E4TF1, responsible for expression of the adenovirus E4 gene. Because of its chromosomal localization and ability to form heterodimers with other polypeptides, this gene may play a role in the Down Syndrome phenotype.