Thermo Fisher Scientific IHH Monoclonal Antibody (363CT4.1.6)
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Applications
Tested Dilution
Publications
Western Blot (WB)
1:500-1:8,000
Product Specifications
Species Reactivity
Human
Host/Isotype
Mouse / IgG3
Class
Monoclonal
Type
Antibody
Clone
363CT4.1.6
Immunogen
KLH conjugated synthetic peptide selected from the C-terminal region of human IHH if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
IHH,
uniProtId:
Q14623-1,
ncbiNodeId:
9606,
antigenRange:
411,
antigenLength:
411,
antigenImageFileName:
MA5-37541_IHH_Q14623-1_House_mouse.svg,
antigenImageFileNamePDP:
MA5-37541_IHH_Q14623-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
Conc. Not Determined
Storage buffer
ascites, pH 7.4
Contains
0.09% sodium azide
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions
Wet ice
RRID
AB_2897471
Target Information
Ihh encodes a member of the hedgehog family of secreted signaling molecules. Hedgehog proteins are essential regulators of a variety of developmental processes including growth, patterning and morphogenesis. The encoded protein specifically plays a role in bone growth an differentiation. Mutations in this gene are the cause of brachydactyly type A1 which is characterized by shortening or malformation of the phalanges. Mutations in this gene are also the cause of acrocapitofemoral dysplasia.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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