
Thermo Fisher Scientific EVC2 Polyclonal Antibody
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Applications
Tested Dilution
Publications
Western Blot (WB)
0.5 µg/mL
Immunohistochemistry (Paraffin) (IHC (P))
2-4 µg/mL
Product Specifications
Species Reactivity
Human
Host/Isotype
Goat / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Peptide with sequence C-LNAKKAMRALGMD. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
EVC2,
uniProtId:
Q86UK5-1,
ncbiNodeId:
9606,
antigenRange:
1296-1308,
antigenLength:
1308,
antigenImageFileName:
PA5-142050_EVC2_Q86UK5-1_Goat.svg,
antigenImageFileNamePDP:
PA5-142050_EVC2_Q86UK5-1_Goat_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.5 mg/mL
Purification
Ammonium sulfate precipitation
Storage buffer
TBS, pH 7.3, with 0.5% BSA
Contains
0.02% sodium azide
Storage conditions
-20° C, Avoid Freeze/Thaw Cycles
Shipping conditions
Wet ice
RRID
AB_2932713
Product Specific Information
Additional Information: This antibody is expected to recognise isoform 1 (NP_667338.3) and isoform 2 (NP_001159608.1).
This antibody is tested in Peptide ELISA: antibody detection limit dilution 1:16,000.
Target Information
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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