EVC2 Polyclonal Antibody

CAT: 0866-RD76830A-01Size: 20 µLDry Ice: NoHazardous: No
CAT#:0866-RD76830A-01Size:20 µL
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Background
This gene encodes a protein that functions in bone formation and skeletal development. Mutations in this gene, as well as in a neighboring gene that lies in a head-to-head configuration, cause Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia that is also known as chondroectodermal dysplasia. Mutations in this gene also cause acrofacial dysostosis Weyers type, also referred to as Curry-Hall syndrome, a disease that combines limb and facial abnormalities. Alternative splicing results in multiple transcript variants.
Description
This is a EVC2 Polyclonal Antibody from Reddot Biotech. This product is for Research Use Only.
Synonyms
Ellis van Creveld syndrome 2, LBN, Limbin
Swiss Prot
Q86UK5
Accession Number
NP_667338
Reactivity
Human
Immunogen
Synthetic peptide of human EVC2
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Polyclonal Antibody
Applications
IHC, ELISA
Purification Method
Affinity purification
Assay Type
Antibody
Concentration
1 mg/mL
Dilution
IHC 1:50-1:200
Buffer
PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Storage Conditions
Store at -20°C. Avoid freeze / thaw cycles.
Host or Source
Rabbit
Isotype
IgG

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