- Phare
- Validé par KD/KO
Anticorps Polyclonal de lapin anti-IFT20
IFT20 Polyclonal Antibody for WB, IHC, IF/ICC, IP, ELISA
Hôte / Isotype
Lapin / IgG
Réactivité testée
canin, Humain, rat, souris et plus (1)
Applications
WB, IHC, IF/ICC, IP, CoIP, ELISA
Conjugaison
Non conjugué
N° de cat : 13615-1-AP
Synonymes
Galerie de données de validation
Applications testées
| Résultats positifs en WB | cellules HEK-293, cellules MDCK, tissu testiculaire de rat, tissu testiculaire de souris | 
| Résultats positifs en IP | tissu testiculaire de souris | 
| Résultats positifs en IHC | tissu de cancer de l'endomètre humain il est suggéré de démasquer l'antigène avec un tampon de TE buffer pH 9.0; (*) À défaut, 'le démasquage de l'antigène peut être 'effectué avec un tampon citrate pH 6,0. | 
| Résultats positifs en IF/ICC | cellules hTERT-RPE1, cellules MDCK | 
Dilution recommandée
| Application | Dilution | 
|---|---|
| Western Blot (WB) | WB : 1:300-1:800 | 
| Immunoprécipitation (IP) | IP : 0.5-4.0 ug for 1.0-3.0 mg of total protein lysate | 
| Immunohistochimie (IHC) | IHC : 1:20-1:200 | 
| Immunofluorescence (IF)/ICC | IF/ICC : 1:20-1:200 | 
| It is recommended that this reagent should be titrated in each testing system to obtain optimal results. | |
| Sample-dependent, check data in validation data gallery | |
Informations sur le produit
13615-1-AP cible IFT20 dans les applications de WB, IHC, IF/ICC, IP, CoIP, ELISA et montre une réactivité avec des échantillons canin, Humain, rat, souris
| Réactivité | canin, Humain, rat, souris | 
| Réactivité citée | rat, canin, Humain, poisson-zèbre, souris | 
| Hôte / Isotype | Lapin / IgG | 
| Clonalité | Polyclonal | 
| Type | Anticorps | 
| Immunogène | IFT20 Protéine recombinante Ag4521 | 
| Nom complet | intraflagellar transport 20 homolog (Chlamydomonas) | 
| Masse moléculaire calculée | 15 kDa | 
| Poids moléculaire observé | 15-18 kDa | 
| Numéro d’acquisition GenBank | BC038094 | 
| Symbole du gène | IFT20 | 
| Identification du gène (NCBI) | 90410 | 
| Conjugaison | Non conjugué | 
| Forme | Liquide | 
| Méthode de purification | Purification par affinité contre l'antigène | 
| Tampon de stockage | PBS with 0.02% sodium azide and 50% glycerol | 
| Conditions de stockage | Stocker à -20°C. Stable pendant un an après l'expédition. L'aliquotage n'est pas nécessaire pour le stockage à -20oC Les 20ul contiennent 0,1% de BSA. | 
Informations générales
Intraflagellar transport (IFT), mediated by molecular motors and IFT particles, is an important transport process that occurs in the cilium. IFT particles are multi-subunit complexes that are made up of complex A and complex B. IFT20 is a component of IFT complex B and involved in ciliary process assembly. It is associated with the Golgi complex and plays a role in the trafficking of ciliary membrane proteins from the Golgi complex to the cilium.
Protocole
| Product Specific Protocols | |
|---|---|
| WB protocol for IFT20 antibody 13615-1-AP | Download protocol | 
| IHC protocol for IFT20 antibody 13615-1-AP | Download protocol | 
| IF protocol for IFT20 antibody 13615-1-AP | Download protocol | 
| IP protocol for IFT20 antibody 13615-1-AP | Download protocol | 
| Standard Protocols | |
|---|---|
| Click here to view our Standard Protocols | 
Publications
| Species | Application | Title | 
|---|---|---|
| Nat Cell Biol Early steps in primary cilium assembly require EHD1/EHD3-dependent ciliary vesicle formation. | ||
| Nat Cell Biol Early steps in primary cilium assembly require EHD1/EHD3-dependent ciliary vesicle formation. | ||
| Sci Adv An EMT-primary cilium-GLIS2 signaling axis regulates mammogenesis and claudin-low breast tumorigenesis. | ||
| Nat Commun Microtubule asters anchored by FSD1 control axoneme assembly and ciliogenesis. | ||
| Proc Natl Acad Sci U S A EMT programs promote basal mammary stem cell and tumor-initiating cell stemness by inducing primary ciliogenesis and Hedgehog signaling.
 | 
Avis
The reviews below have been submitted by verified Proteintech customers who received an incentive for providing their feedback.
| FH Charlotte (Verified Customer) (07-18-2024) | I did the standard iF protocol on the classic LIGHT2 cells used to study Hh signalling that depends on the primary cilia: PFA 4% 10 min cold methanol 5 min 1h in 1% BSA in PBST 1/150 in blocking solution, O.N. at 4°C 5*5min PBST 1/500 in blocking solution, 1h at RT° 4*5min PBST + 5min PBS I'm not convinced as the background is super dotty and quite important. Maybe the conditions must be optimized but it doesn't look promising 
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| FH kes (Verified Customer) (01-17-2022) | I used it for WB(1:1000) and IF for cilia (1:200) and got good results. 
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| FH Boyan (Verified Customer) (03-15-2019) | Excellent for IF labelling of the Golgi under PFA fixation. 
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