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CCM2 antibody
CCM2
Reactivity: Human, Mouse, Rat
IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-CCM2 Antibody
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Target
See all CCM2 Antibodies
CCM2
(Cerebral Cavernous Malformation 2 (CCM2))
Reactivity
All reactivities for CCM2 antibodies
Human, Mouse, Rat
Host
All hosts for CCM2 antibodies
Rabbit
Clonality
All clonalities for CCM2 antibodies
Polyclonal
Conjugate
All conjugates for CCM2 antibodies
This CCM2 antibody is un-conjugated
Application
All applications for CCM2 antibodies
Immunohistochemistry (IHC)
Characteristics
Polyclonal Antibody
Purification
Affinity purification
Immunogen
Recombinant fusion protein of human CCM2 (NP_113631.1).
Isotype
IgG
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Discover our top product CCM2 Primary Antibody
Alternatives
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Application Details
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Application Notes
IHC 1:50-1:200
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
1 mg/mL
Buffer
PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
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 CCM2
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Target
CCM2
(Cerebral Cavernous Malformation 2 (CCM2))
Alternative Name
CCM2 (CCM2 Products )
Synonyms
C7orf22 antibody, OSM antibody, malcavernin antibody, CCM2 antibody, BC029157 antibody, TUF2 antibody, vtn antibody, zgc:110233 antibody, CCM2 scaffolding protein antibody, cerebral cavernous malformation 2 antibody, malcavernin antibody, CCM2 antibody, Ccm2 antibody, LOC100304744 antibody, ccm2 antibody
Background
This gene encodes a scaffold protein that functions in the stress-activated p38 Mitogen-activated protein kinase (MAPK) signaling cascade. The protein interacts with SMAD specific E3 ubiquitin protein ligase 1 (also known as SMURF1) via a phosphotyrosine binding domain to promote RhoA degradation. The protein is required for normal cytoskeletal structure, cell-cell interactions, and lumen formation in endothelial cells. Mutations in this gene result in cerebral cavernous malformations. Multiple transcript variants encoding different isoforms have been found for this gene.
Gene ID
83605
UniProt
Q9BSQ5
Pathways
Cell-Cell Junction Organization
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