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:
-
- Data
- Citations
- Publication
- Sequence / 3D
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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.
Database link
Valid Sequence:
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."
[10].
"Novel mutations of ABCB6 associated with autosomal dominant dyschromatosis universalis hereditaria."
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