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The protein encoded by ABCB8 belongs to the family of cytoplasmic linker proteins, which have been proposed to mediate the interaction between specific membranous organelles and microtubules. Zusätzlich bieten wir Ihnen ATP-Binding Cassette, Sub-Family B (MDR/TAP), Member 8 Antikörper (41) und ATP-Binding Cassette, Sub-Family B (MDR/TAP), Member 8 Proteine (5) und viele weitere Produktgruppen zu diesem Protein an.
Cross checking with epidemiological estimates and model validation suggests that CLIP2 (zeige CLIP2 ELISA Kits) is a marker of high precision. CLIP2 (zeige CLIP2 ELISA Kits) leaves an imprint in the epidemiological incidence data which is typical for a driver gene.
CLIP2 (zeige CLIP2 ELISA Kits) protein expression is elevated in papillary thyroid carcinomas from patients exposed to radioiodine fallout compared with a nonexposed control group.
A clear radiation dose-response relationship for the CLIP2 (zeige CLIP2 ELISA Kits) marker expression in post-Chernobyl papillary thyroid carcinomas
CLIP2 (zeige CLIP2 ELISA Kits) haploinsufficiency by itself does not lead to the physical or cognitive characteristics of the Williams-Beuren syndrome; GTF2IRD1 and GTF2I (zeige GTF2I ELISA Kits) are the main genes causing the cognitive defects
Data show that gene CLIP2 (zeige CLIP2 ELISA Kits) was specifically overexpressed in the exposed cases.
ABCB8 confers resistance through the protection of mitochondrial DNA from doxorubicin-induced DNA damage in a melanoma cell line.
mutations in ABCB8 and ABCB10 (zeige ABCB10 ELISA Kits) is not associated with acute myeloid leukemia (zeige BCL11A ELISA Kits).
These results indicate that ABCB8 is essential for normal cardiac function, maintenance of mitochondrial iron homeostasis and maturation of cytosolic Fe/S proteins.
The protein encoded by this gene belongs to the family of cytoplasmic linker proteins, which have been proposed to mediate the interaction between specific membranous organelles and microtubules. This protein was found to associate with both microtubules and an organelle called the dendritic lamellar body. This gene is hemizygously deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants.
ATP-binding cassette sub-family B member 8, mitochondrial
, mitochondrial ABC protein
, mitochondrial ATP-binding cassette 1
, CAP-Gly domain-containing linker protein 2
, Williams-Beuren syndrome chromosome region 3
, Williams-Beuren syndrome chromosome region 4
, cytoplasmic linker 2
, cytoplasmic linker protein 115
, cytoplasmic linker protein 2
, williams-Beuren syndrome chromosomal region 3 protein
, williams-Beuren syndrome chromosomal region 4 protein
, ABC transporter 8
, ATP-binding cassette, sub-family B (MDR/TAP), member 8
, ATP-binding cassette, sub-family B, member 8
, ATP-binding cassette sub-family B member 8, mitochondrial-like