Btk, Human Antibody from MILTENYI BIOTEC B.V. & Co. KG

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Antigenic SpecificityBtk, Human
CloneREA367
Host SpeciesRecombinant Human
Reactive Specieshuman
IsotypeIgG1
Formatphycoerythrin (PE) conjugate
Size30 tests in 60 µL
Concentration1:50
ApplicationsIntracellular flow cytometry
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DescriptionBtk Antibody, anti-human, PE, REAfinity™. Clone REA367 recognizes the human bruton tyrosine kinase (Btk) antigen, a non-receptor tyrosine kinase belonging to the Tec family of kinases. Btk is critical for B cell-development, -differentiation, and -signaling. Moreover, Btk expression is assumed to be a prerequisite for B cell-proliferation and -survival. Consequently, Btk-deficient B lymphocytes fail to reach the mature state and are presumably doomed to premature death. Btk is reported to be associated with human disease. Thus, individuals harboring loss-of-function mutations in the gene encoding Btk virtually lack circulating B lymphocytes, are unable to generate immunoglobulins of all classes, and therefore cannot mount humoral immune responses. This primary immunodeficiency is named X-linked agammaglobulinemia. | Additional information: Clone REA367 displays negligible binding to Fc receptors.
Immunogenn/a
Other NamesAGMX1, AT, ATK, BPK, IMD1, PSCTK1, XLA
Gene, Accession #Gene ID: 695
Catalog #130-116-669
Price$119
Order / More InfoBtk, Human Antibody from MILTENYI BIOTEC B.V. & Co. KG
Product Specific ReferencesVetrie, D. et al. (1993) The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases. Nature 361 (6409): 226-233. | Tsukada, S. et al. (1993) Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia. Cell 72 (2): 279-290. | Mohamed, A. J. et al. (2009) Bruton's tyrosine kinase (Btk): function, regulation, and transformation with special emphasis on the PH domain. Immunol. Rev. 228 (1): 58-73.
MILTENYI BIOTEC B.V. & Co. KG
MILTENYI BIOTEC B.V. & Co. KG
MILTENYI BIOTEC B.V. & Co. KG
Friedrich-Ebert-Straße 68
51429 Bergisch Gladbach GERMANY
P: +49 2204 8306-0
F: +49 2204 85197

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