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WNT1 Polyclonal Antibody Host Rabbit

SKU: E-AB-33231-200

  • $ 55995


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WNT1 Polyclonal Antibody Host Rabbit

 

SKU # E-AB-33231
Reactivity Human, Mouse
Host Rabbit
Applications WB, IHC-p, IF

 

Product Details

Isotype IgG
Host Rabbit
Reactivity Human, Mouse
Applications WB, IHC-p, IF
Clonality Polyclonal
Immunogen Synthesized peptide derived from the C-terminal region of human Wnt-1
Abbre Wnt-1
Synonyms BMND16,  INT1,  OI15,  Proto oncogene protein Wnt 1,  Proto-oncogene Int-1 homolog,  Proto-oncogene Wnt-1,  WNT1,  Wingless type MMTV integration site family member 1,  Wnt 1,  member 1 (oncogene INT1),  oncogene Int1,  wingless-type MMTV integration site family,  wnt1
Swissprot
Calculated MW 41 kDa
Observed MW 45 kDa
Cellular Localization Secreted>extracellular space>extracellular matrix.
Concentration 1 mg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer, 0.5% protein protectant and 50% glycerol.
Purification Method Affinity purification
Research Areas Cancer,  Stem Cells
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack, upon receipt, store it immediately at the temperature recommended.

 

Related Reagents

Applications Recommended Dilution
WB 1:500-1:2000
IHC  1:100-1:300
IF 1:200-1:1000

 

Background

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. This gene is a member of the WNT gene family. It is very conserved in evolution, and the protein encoded by this gene is known to be 98% identical to the mouse Wnt1 protein at the amino acid level. The 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. This gene is clustered with another family member, WNT10B, in the chromosome 12q13 region.