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BioWhittaker Molecular Applications liquid culture imdm
Liquid Culture Imdm, supplied by BioWhittaker Molecular Applications, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/liquid+culture+imdm/liquid+culture+imdm/pm12591280-65-0-11
Average 90 stars, based on 1 article reviews
liquid culture imdm - by Bioz Stars, 2026-10
90/100 stars

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Related Articles

Recombinant:

Article Title: X-linked thrombocytopenia caused by a mutation in the Wiskott-Aldrich syndrome (WAS) gene that disrupts interaction with the WAS protein (WASP)-interacting protein (WIP).
Article Snippet: Objective.. We studied two adult brothers with severe congenital thrombocytopenia in order to determine the genetic etiology of their inherited disorder.. Despite the absence of eczema or immunodeficiency, a mutation of the Wiskott-Aldrich syndrome (WAS) gene was suspected because of the presence of microthrombocytes.

Isolation:

Article Title: X-linked thrombocytopenia caused by a mutation in the Wiskott-Aldrich syndrome (WAS) gene that disrupts interaction with the WAS protein (WASP)-interacting protein (WIP).
Article Snippet: Objective.. We studied two adult brothers with severe congenital thrombocytopenia in order to determine the genetic etiology of their inherited disorder.. Despite the absence of eczema or immunodeficiency, a mutation of the Wiskott-Aldrich syndrome (WAS) gene was suspected because of the presence of microthrombocytes.

Modification:

Article Title: X-linked thrombocytopenia caused by a mutation in the Wiskott-Aldrich syndrome (WAS) gene that disrupts interaction with the WAS protein (WASP)-interacting protein (WIP).
Article Snippet: Objective.. We studied two adult brothers with severe congenital thrombocytopenia in order to determine the genetic etiology of their inherited disorder.. Despite the absence of eczema or immunodeficiency, a mutation of the Wiskott-Aldrich syndrome (WAS) gene was suspected because of the presence of microthrombocytes.

Incubation:

Article Title: X-linked thrombocytopenia caused by a mutation in the Wiskott-Aldrich syndrome (WAS) gene that disrupts interaction with the WAS protein (WASP)-interacting protein (WIP).
Article Snippet: Objective.. We studied two adult brothers with severe congenital thrombocytopenia in order to determine the genetic etiology of their inherited disorder.. Despite the absence of eczema or immunodeficiency, a mutation of the Wiskott-Aldrich syndrome (WAS) gene was suspected because of the presence of microthrombocytes.

Chloramphenicol Acetyltransferase Assay:

Article Title: X-linked thrombocytopenia caused by a mutation in the Wiskott-Aldrich syndrome (WAS) gene that disrupts interaction with the WAS protein (WASP)-interacting protein (WIP).
Article Snippet: Objective.. We studied two adult brothers with severe congenital thrombocytopenia in order to determine the genetic etiology of their inherited disorder.. Despite the absence of eczema or immunodeficiency, a mutation of the Wiskott-Aldrich syndrome (WAS) gene was suspected because of the presence of microthrombocytes.

Enzyme-linked Immunosorbent Assay:

Article Title: X-linked thrombocytopenia caused by a mutation in the Wiskott-Aldrich syndrome (WAS) gene that disrupts interaction with the WAS protein (WASP)-interacting protein (WIP).
Article Snippet: Objective.. We studied two adult brothers with severe congenital thrombocytopenia in order to determine the genetic etiology of their inherited disorder.. Despite the absence of eczema or immunodeficiency, a mutation of the Wiskott-Aldrich syndrome (WAS) gene was suspected because of the presence of microthrombocytes.



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