×
For best experience we recommend to activate Javascript in your browser.
ZEB2 antibody (AA 750-800)
This Rabbit Polyclonal antibody specifically detects ZEB2 in IHC. It exhibits reactivity toward Human and Mouse.
Quick Overview for ZEB2 antibody (AA 750-800) (ABIN7448878)
Target
See all ZEB2 Antibodies
ZEB2
(Zinc Finger E-Box Binding Homeobox 2 (ZEB2))
Reactivity
All reactivities for ZEB2 antibodies
Human, Mouse
Host
All hosts for ZEB2 antibodies
Rabbit
Clonality
All clonalities for ZEB2 antibodies
Polyclonal
Conjugate
All conjugates for ZEB2 antibodies
This ZEB2 antibody is un-conjugated
Application
All applications for ZEB2 antibodies
Immunohistochemistry (IHC)
Product Details anti-ZEB2 Antibody
(hide)
Binding Specificity
All epitopes for ZEB2 antibodies
AA 750-800
Purpose
Rabbit anti-ZEB2/SIP IHC Antibody, Affinity Purified
Predicted Reactivity
Bovine,Dog,Horse,Rabbit,Pig,Panda,Orangutan,Monkey,Gorilla,Chimpanzee,Ferret,White-tufted-ear marmoset,Thirteen-lined ground squirrel,Small-eared galago,Naked mole rat,Crab-eating macaque,Northern white-cheeked gibbon,Little brown bat
Purification
Affinity Purified
Immunogen
Between AA 750 and 800
Isotype
IgG
Alternatives
(show)
Application Details
(hide)
Application Notes
1:100 - 1:500
Restrictions
For Research Use only
Handling
(hide)
Concentration
250 μg/mL
Buffer
Tris-buffered Saline containing 0.1 % BSA and 0.09 % Sodium Azide
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
4 °C
Expiry Date
12 months
Target Details for ZEB2
(hide)
Target
ZEB2
(Zinc Finger E-Box Binding Homeobox 2 (ZEB2))
Alternative Name
ZEB2/SIP
Background
Background: Smad interacting protein 1 (SIP1) is a transcriptional inhibitor that binds to the DNA sequence, 5'-CACCT-3', in different promoters. SIP1 has been shown to repress the transcription of E-cadherin. Defects in the gene which encodes for SIP1, ZEB2, are the cause of Hirschsprung disease-mental retardation syndrome (Hirschsprung disease) also known as Mowat-Wilson syndrome (MWS). Hirschsprung disease is a rare autosomal dominant complex developmental disorder [taken from the Universal Protein Resource (UniProt) O60315].
Gene ID
9839
NCBI Accession
NP_055610
UniProt
O60315
Pathways
Tube Formation
Recently viewed
(hide)
Chat with us , powered by LiveChat