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WNT1 Monoclonal antibody

WNT1 Monoclonal Antibody for ELISA
Cat No. 66432-1-Ig
Clone No.1E3C10

Host / Isotype

Mouse / IgG2a

Reactivity

human, mouse, rat

Applications

ELISA

INT1, Proto oncogene Int 1 homolog, Proto oncogene Wnt 1, WNT1

Formulation:  PBS and Azide
PBS and Azide
Conjugate:  Unconjugated
Size/Concentration: 

-/ -


ご購入について

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国内在庫・納期について

約2万点のプロテインテック製品をコスモバイオ社物流センター(国内)に在庫しています。国内在庫の有無はコスモバイオ社ホームページの「品番検索」でカタログ番号を検索して確認できます。


保証・サポートについて

テクニカルサポートまたはご購入後1年間の交換/補填対応を承ります。詳細はこちらをご覧ください。


Tested Applications

Recommended dilution

ApplicationDilution
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.

Product Information

66432-1-Ig targets WNT1 in ELISA applications and shows reactivity with human, mouse, rat samples.

Tested Reactivity human, mouse, rat
Host / Isotype Mouse / IgG2a
Class Monoclonal
Type Antibody
Immunogen WNT1 fusion protein Ag25463 相同性解析による交差性が予測される生物種
Full Name wingless-type MMTV integration site family, member 1
Observed molecular weight 41 kDa
GenBank accession numberBC074799
Gene Symbol WNT1
Gene ID (NCBI) 7471
Conjugate Unconjugated
Form Liquid
Purification MethodProtein A purification
UNIPROT IDP04628
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol , pH 7.3
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

Background Information

WNT1 is a member of the WNT gene family. WNT1 have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. 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. 

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