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Contactin 4 antibody
CNTN4
Reactivity: Human, Mouse, Rat
ELISA, IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-Contactin 4 Antibody
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Target
See all Contactin 4 (CNTN4) Antibodies
Contactin 4 (CNTN4)
Reactivity
Human, Mouse, Rat
Host
All hosts for Contactin 4 antibodies
Rabbit
Clonality
All clonalities for Contactin 4 antibodies
Polyclonal
Conjugate
All conjugates for Contactin 4 antibodies
This Contactin 4 antibody is un-conjugated
Application
All applications for Contactin 4 antibodies
ELISA, Immunohistochemistry (IHC)
Characteristics
Polyclonal Antibody
Purification
Antigen affinity purification
Immunogen
Fusion protein of human CNTN4
Isotype
IgG
Top Product
Discover our top product CNTN4 Primary Antibody
Alternatives
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Application Details
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Application Notes
IHC 1:50-1:200, ELISA 1:5000-1:10000
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
1.14 mg/mL
Buffer
PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
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
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for Contactin 4
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Target
Contactin 4 (CNTN4)
Alternative Name
CNTN4 (CNTN4 Products )
Synonyms
Axcam antibody, Big-2 antibody, AXCAM antibody, BIG-2 antibody, 9630050B05 antibody, FAR-1 antibody, MGC84491 antibody, zgc:153573 antibody, axcam antibody, big-2 antibody, cntn4a antibody, contactin 4 antibody, contactin 4 S homeolog antibody, Cntn4 antibody, CNTN4 antibody, cntn4.S antibody, cntn4 antibody
Background
This gene encodes a member of the contactin family of immunoglobulins. Contactins are axon-associated cell adhesion molecules that function in neuronal network formation and plasticity. The encoded protein is a glycosylphosphatidylinositol-anchored neuronal membrane protein that may play a role in the formation of axon connections in the developing nervous system. Deletion or mutation of this gene may play a role in 3p deletion syndrome and autism spectrum disorders. Alternative splicing results in multiple transcript variants.
UniProt
Q8IWV2
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