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Abcb6 (GeneName), ATP-binding cassette sub-family B member 6, mitochondrial (ProteinName), ABCB6_MOUSE.
Product Name:

Mouse Abcb6/ ATP-binding cassette sub-family B member 6, mitochondrial ELISA Kit

Cat.#:
-
Brand:
EIAab®
Regulatory Status:
Detection Method:
ELISA
Specificity:
Natural and recombinant mouse ATP-binding cassette sub-family B member 6, mitochondrial
Sample Type:
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Sample Data:
Research Area:
-
Mouse Abcb6 ELISA Kit
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Mouse Abcb6 ELISA Kit
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Product Datasheets


General Annotation


Sub Unit:
Homodimer.


Function:
Binds heme and porphyrins and functions in their ATP-dependent uptake into the mitochondria. Plays a crucial role in heme synthesis.


Subcellular Location:
Cell membrane Multi-pass membrane protein Mitochondrion outer membrane Multi-pass membrane protein Endoplasmic reticulum membrane Multi-pass membrane protein Golgi apparatus membrane Multi-pass membrane protein Endosome membrane Multi-pass membrane protein localized to the endosome-like compartement and dendrite tips.


This product has not yet been referenced specifically in any publications.

[1].
"Human ABC transporter isoform B6 (ABCB6) localizes primarily in the Golgi apparatus."

[2].
"Isolation of a genomic clone containing the promoter region of the human ATP binding cassette (ABC) transporter, ABCB6."

[3].
"ABCB6 (MTABC3) excluded as the causative gene for the growth retardation syndrome with aminoaciduria, cholestasis, iron overload, and lactacidosis."

[4].
"MTABC3, a novel mitochondrial ATP-binding cassette protein involved in iron homeostasis."

[5].
"Familial pseudohyperkalemia in blood donors: a novel mutation with implications for transfusion practice."

[6].
"Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria."

[7].
"Novel missense mutations of ABCB6 in two chinese families with dyschromatosis universalis hereditaria."

[8].
"Missense mutations in the ABCB6 transporter cause dominant familial pseudohyperkalemia."

[9].
"Mutations in ABCB6 cause dyschromatosis universalis hereditaria."

[10].
"Novel mutations of ABCB6 associated with autosomal dominant dyschromatosis universalis hereditaria."
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