![PE Anti-Human CD197/CCR7 Antibody [G043H7] - E-AB-F1159D Microglial Cells Defects in MYOZ2 are the](https://cdn.shopify.com/s/files/1/0305/9482/6376/products/logo_new_84ecf773-ea92-45dc-98aa-c5ba58b6dafd.png?v=1710511701){kind=logo}
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Defects in MYOZ2 are the cause of familial hypertrophic cardiomyopathy type 16 (CMH16)
The complex is then transported across the cell to be secreted at the apical surface
Alternative Name: LDLCQ3
and the second is a Ca2+-dependent carbohydrate binding domain at the very C-terminus that is unusually stabilized by three ions
Catalogue Numbers: E-EL-H0702-24T
PE Anti-Human CD197/CCR7 Antibody [G043H7] - E-AB-F1159D Microglial Cells Defects in MYOZ2 are thePE Anti Human CD197 CCR7 Antibody [G043H7] Sizes: 100 Tests, 100 Tests2 Catalogue Numbers: E AB F1159D 100, E AB F1159D 1002 Citations, Manuals and MSDS Available upon request. Abbreviation: CD197 Target Synonym: CMKBR7, EBI1, EVI1, CCR 7, CDw197, Conjugation: PE Host: Mouse Species Reactivity: Human Application: FCM Usage: Each lot of this antibody is quality control tested by flow cytometric analysis. The amount of the reagent is suggested to be