Thermo Fisher Scientific Ihh Polyclonal Antibody
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Applications
Tested Dilution
Publications
Western Blot (WB)
1:1,000-1:3,000
Immunocytochemistry (ICC/IF)
1:100-1:500
Product Specifications
Species Reactivity
Human, Mouse, Non-human primate, Rat
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
A synthesized peptide derived from human IHH(Accession Q14623), corresponding to amino acid residues K108-R158. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
IHH,
uniProtId:
Q14623-1,
ncbiNodeId:
9606,
antigenRange:
108-158,
antigenLength:
411,
antigenImageFileName:
PA5-115399_IHH_Q14623-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-115399_IHH_Q14623-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1 mg/mL
Purification
Affinity chromatography
Storage buffer
PBS with 50% glycerol
Contains
0.02% sodium azide
Storage conditions
-20°C
Shipping conditions
Wet ice
RRID
AB_2900035
Product Specific Information
Antibody detects endogenous levels of total IHH.
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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