Human F7 Antibody Pair Set (E-KAB-0540)

For research use only.
Background |
This gene encodes coagulation factor VII which is a vitamin K-dependent factor essential for hemostasis. This factor circulates in the blood in a zymogen form , and is converted to an active form by either factor IXa , factor Xa , factor XIIa , or thrombin by minor proteolysis. Upon activation of the factor VII , a heavy chain containing a catalytic domain and a light chain containing 2 EGF-like domains are generated , and two chains are held together by a disulfide bond. In the presence of factor III and calcium ions , the activated factor then further activates the coagulation cascade by converting factor IX to factor IXa and/or factor X to factor Xa. Defects in this gene can cause coagulopathy. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.
|
Synonyms |
FVII, Proconvertin, SPCA
|
Swissprot | |
Reactivity |
Human
|
Specificity |
Detects Human F7 in ELISAs
|
Applications |
ELISA
|
Storage |
-20℃
|
Expiration date |
12 months
|
Other Clones
{{antibodyDetailsPage.numTotal}} Results
-
{{item.title}}
Citations ({{item.publications_count}}) Manual MSDS
Cat.No.:{{item.cat}}
{{index}} {{goods_show_value}}
Other Formats
{{formatDetailsPage.numTotal}} Results
-
{{item.title}}
Citations ({{item.publications_count}}) Manual MSDS
Cat.No.:{{item.cat}}
{{index}} {{goods_show_value}}
-
IF:{{item.impact}}
Journal:{{item.journal}} ({{item.year}})
DOI:{{item.doi}}Reactivity:{{item.species}}
Sample Type:{{item.organization}}
-
Q{{(FAQpage.currentPage - 1)*pageSize+index+1}}:{{item.name}}