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FOXC1 Monoclonal antibody, PBS Only

FOXC1 Monoclonal Antibody for WB, Indirect ELISA
Cat No. 66568-1-PBS
Clone No.1F4E11

Host / Isotype

Mouse / IgG1

Reactivity

human

Applications

WB, Indirect ELISA

FREAC 3, Forkhead-related transcription factor 3, Forkhead-related protein FKHL7, FKHL7, ARA

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

-/ -


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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.

Product Information

66568-1-PBS targets FOXC1 in WB, Indirect ELISA applications and shows reactivity with human samples.

Tested Reactivity human
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Immunogen Peptide 相同性解析による交差性が予測される生物種
Full Name forkhead box C1
Calculated molecular weight 57 kDa
Observed molecular weight 70-75 kDa
GenBank accession numberNM_001453
Gene Symbol FOXC1
Gene ID (NCBI) 2296
RRIDAB_2881929
Conjugate Unconjugated
Form Liquid
Purification MethodProtein G purification
UNIPROT IDQ12948
Storage Buffer PBS Only
Storage ConditionsStore at -80°C.

Background Information

FOXC1, also named as FKHL7 and FREAC3, binding of FREAC-3 and FREAC-4 to their cognate sites results in bending of the DNA at an angle of 80-90 degrees. Defects in FOXC1 are the cause of Axenfeld-Rieger syndrome type 3 (RIEG3). Defects in FOXC1 are the cause of iridogoniodysgenesis anomaly (IGDA). Defects in FOXC1 are a cause of Peters anomaly.

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