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|Tested species reactivity||Human|
|Published species reactivity||Not Applicable|
|Host / Isotype||Mouse / IgG1|
|Storage buffer||PBS, pH 7.2|
|Contains||5mM sodium azide|
|Storage Conditions||4° C|
|Antibody Form||Whole Antibody|
|Tested Applications||Dilution *|
* Suggested working dilutions are given as a guide only. It is recommended that the user titrate the product for use in their own experiment using appropriate negative and positive controls.
Anti-Human secondary antibodies are affinity-purified antibodies with well-characterized specificity for human immunoglobulins and are useful in the detection, sorting or purification of its specified target. Secondary antibodies offer increased versatility enabling users to use many detection systems (e.g. HRP, AP, fluorescence). They can also provide greater sensitivity through signal amplification as multiple secondary antibodies can bind to a single primary antibody. Most commonly, secondary antibodies are generated by immunizing the host animal with a pooled population of immunoglobulins from the target species and can be further purified and modified (i.e. immunoaffinity chromatography, antibody fragmentation, label conjugation, etc.) to generate highly specific reagents.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
|Not Applicable||Not Cited||Otologic manifestations of immunoglobulin G4-related disease.||Takagi D,Nakamaru Y,Fukuda S||The Annals of otology, rhinology, and laryngology (123:420)||2014|
Idiopathic cervical fibrosis--a new member of IgG4-related sclerosing diseases: report of 4 cases, 1 complicated by composite lymphoma.
A-10651 was used in immunohistochemistry - paraffin section to report on four cases of idiopathic cervical fibrosis
|Cheuk W,Tam FK,Chan AN,Luk IS,Yuen AP,Chan WK,Hung TC,Chan JK||The American journal of surgical pathology (34:1678)||2010|
IgG4-related hypophysitis: a new addition to the hypophysitis spectrum.
A-10651 was used in immunohistochemistry to discuss variants of hypophysitis.
|Leporati P,Landek-Salgado MA,Lupi I,Chiovato L,Caturegli P||The Journal of clinical endocrinology and metabolism (96:1971)||2011|