0
There are 0 item in your cart
Cart Subtotal $0.00 Checkout
>   Home   >   Products   >   Primary Antibodies   >   Wnt1 Rabbit pAb   

Wnt1 Rabbit pAb

 
Catalog #
ABZ1423
Application
WB, IF, ICC, ELISA, IHC-P
Uniprot Id
P04628
Reactivity
Human, Mouse
Isotype
IgG
 
Be the first to write a review
 
  • Western blot analysis of Wnt1 in various lysates using Wnt1 antibody.
  • Western blot analysis of Wnt1 in HT-29 lysates using Wnt1 antibody.
 Catalog #AvailabilitySizeQuantityUnit Price Save For Later Wish List
ABZ1423-100 2 weeks 100 µL $499.00
Select product before adding to cart
ABZ1423-20 2 weeks 20 µL $149.00
  • Datasheet
  • Citations
  • Reviews

Product Overview

NameWnt1 Rabbit pAb
Accession (Primary)P04628
Host SpeciesRabbit
ClonalityPolyclonal
IsotypeIgG
Species Reactivity
Reacts WithHuman, Mouse
Calculated MW
Calculated MW: 41 kDa; Observed MW: 45 kDa
Buffer System
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide, pH 7.3.
Storage
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Recommended Dilution
WB-1:500-1:2000; IHC-1:100-1:300; IF-1:200-1:1000; ELISA-1:10000
Purification
Affinity Purified
Conjugation
Unconjugated
Modification
Unmodified
Form
Liquid
Background
WNT1: wingless-type MMTV integration site family, member 1. 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 rolein Joubert syndrome. This gene is clustered with another family member, WNT10B, in the chromosome 12q13 region.

Target Information: ( P04628 )

NameWNT1
Gene ID7471
Other Names
WNT1; INT1; Proto-oncogene Wnt-1; Proto-oncogene Int-1 homolog
Citation banner

Thousands of laboratories across the world have published research that depended on the performance of antibodies from ADMEbio to advance their research.
Check out links to articles that cite our products in major peer-reviewed journals, organized by research category.

Thank you,
ADMEbio Team

Citation banner
Be the first to review product

ADMEbio welcomes feedback from our customers.

  • Be seen as an expert in the field of the products you are reviewing
  • Showcase your results (you can upload an image) to the antibody community. New product applications are welcome!
  • Share your experience to help other researchers make more informed decisions.
  • Easy process through our 5 star rating system and single login through your account.

Thank you,
ADMEbio Team






Order Information
Call
760-390-3989
Shipping Information
For shipping outside United State, please contact
sales@admebio.com