FOXN1 anticorps (AA 321-420)
-
- Antigène Voir toutes FOXN1 Anticorps
- FOXN1 (Forkhead Box N1 (FOXN1))
-
Épitope
- AA 321-420
-
Reactivité
- Humain, Rat, Souris
-
Hôte
- Lapin
-
Clonalité
- Polyclonal
-
Conjugué
- Cet anticorp FOXN1 est non-conjugé
-
Application
- Western Blotting (WB), ELISA, Flow Cytometry (FACS), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- Réactivité croisée
- Humain, Souris, Rat
- Homologie
- Dog,Cow,Pig,Horse,Chicken,Rabbit
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human FOXN1
- Isotype
- IgG
-
-
- Indications d'application
-
WB 1:300-5000
ELISA 1:500-1000
FCM 1:20-100
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Restrictions
- For Research Use only
-
- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- Agent conservateur
- ProClin
- Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Stock
- 4 °C,-20 °C
- Stockage commentaire
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- Date de péremption
- 12 months
-
-
EXTL3
mutations cause skeletal dysplasia, immune deficiency, and developmental delay. ..." dans: The Journal of experimental medicine, Vol. 214, Issue 3, pp. 623-637, (2017) (PubMed).
: "
-
EXTL3
mutations cause skeletal dysplasia, immune deficiency, and developmental delay. ..." dans: The Journal of experimental medicine, Vol. 214, Issue 3, pp. 623-637, (2017) (PubMed).
-
- Antigène
- FOXN1 (Forkhead Box N1 (FOXN1))
- Autre désignation
- FOXN1 (FOXN1 Produits)
- Synonymes
- anticorps nude, anticorps whnb, anticorps FOXN1, anticorps foxN1, anticorps foxN, anticorps foxn1, anticorps FKHL20, anticorps RONU, anticorps WHN, anticorps D11Bhm185e, anticorps Fkh19, anticorps HFH-11, anticorps Hfh11, anticorps Whn, anticorps nu, anticorps Rnu, anticorps forkhead box N1, anticorps forkhead box protein N1, anticorps FOXN1, anticorps foxn1, anticorps foxN1, anticorps LOC100125524, anticorps Foxn1
- Sujet
-
Synonyms: WHN, RONU, FKHL20, Forkhead box protein N1, Winged-helix transcription factor nude, FOXN1
Background: Mutations in the winged-helix transcription factor gene at the nude locus in mice and rats produce the pleiotropic phenotype of hairlessness and athymia, resulting in a severely compromised immune system. This gene is orthologous to the mouse and rat genes and encodes a similar DNA-binding transcription factor that is thought to regulate keratin gene expression. A mutation in this gene has been correlated with T-cell immunodeficiency, the skin disorder congenital alopecia, and nail dystrophy. Alternative splicing in the 5' UTR of this gene has been observed. [provided by RefSeq, Jul 2008].
- ID gène
- 8456
- UniProt
- O15353
-