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  2. Polyclonal

600-401-A37

Wnt1 Antibody

Eine Lieferung in diese Region ist nicht möglich.

SKU:
600-401-A37
Zusätzliche Namen:
rabbit anti-WNT-1 antibody, rabbit anti-WNT1 antibody, INT1 antibody, Murine mammary tumor virus integration site 1 antibody, Oncogene INT1 antibody, Proto oncogene protein Wnt 1 antibody, Wingless type MMTV integration site family member 1 antibody|WNT1
Anwendung:
ELISA, WB
Konzentration:
1 mg/ml
Physischer Zustand:
Liquid
Spezies-Reaktivität:
Human
Lagerbedingungen:
-20[o]C aliquoted. Aliquot. Avoid freeze/thaw cycles., 2-8[o]C diluted. Aliquot. Avoid freeze/thaw cycles.
Hersteller:
Rockland Inc
Host:
Rabbit
Reaktivitäten:
Human, Mouse
Buffer:
0.02 M Potassium Phosphate, 0.15 M Sodium Chloride
Immunogen:
This affinity purified antibody was prepared from whole rabbit serum produced by repeated immunizations with a synthetic peptide corresponding to an internal region of human Wnt1 protein.
Formulierung:
0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2
Uniprot:
P04628
Synonyme:
BMND16;INT1;OI15;proto-oncogene Int-1 homolog;proto-oncogene Wnt-1;wingless-type MMTV integration site family member 1;wingless-type MMTV integration site family, member 1 (oncogene INT1)
Weitere Details:
The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. Wnt1 (Wingless-type MMTV integration site family member 1) is a member of the WNT gene family. It is highly conserved in evolution and the protein encoded by this gene is known to be 98% identical to mouse Wnt1 protein at the amino acid level. Studies in mouse indicate that the Wnt1 protein functions in the induction of the mesencephalon and cerebellum. This gene was originally considered as a candidate gene for Joubert syndrome, an autosomal recessive disorder with cerebellar hypoplasia as a leading feature. However, further studies suggested that the gene mutations might not have a significant role in Joubert syndrome. Wnt1 is secreted as an extracellular matrix protein.
Versandbedingungen:
Dry Ice