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ABCB7 (GeneName), ATP-binding cassette sub-family B member 7, mitochondrial (ProteinName), ABCB7_HUMAN.

Product Name:

Human ABCB7/ ATP-binding cassette sub-family B member 7, mitochondrial ELISA Kit

Cat.#:

Brand:

EIAab^®

Regulatory Status:

RUO

Alternative:

ATP-binding cassette transporter 7, ABC transporter 7 protein, ABC7

Detection Method:

ELISA

Specificity:

Natural and recombinant human ATP-binding cassette sub-family B member 7, mitochondrial

Sample Type:

Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids

Sample Data:

Research Area:

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Human ABCB7 ELISA Kit

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Product Datasheets

Data
Citations
Publication
Sequence / 3D
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General Annotation

Sub Unit:

Homodimer or heterodimer.

Function:

Could be involved in the transport of heme from the mitochondria to the cytosol. Plays a central role in the maturation of cytosolic iron-sulfur (Fe/S) cluster-containing proteins.

Subcellular Location:

Mitochondrion inner membrane Multi-pass membrane protein

Database link

UniGene:

Hs.370480

SMR:

O75027

STRING:

9606.ENSP00000253577

KEGG:

hsa:22

MIM:

300135

Pfam:

PF00664

Uniprot:

O75027

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Sequence length:

752

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752:

3D Structure:

Predicted Epitope:

Valid Sequence:

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

[1].

"X-linked cerebellar ataxia and sideroblastic anaemia associated with a missense mutation in the ABC7 gene predicting V411L."

(PMID: 11843825)

[2].

"Human ABC7 transporter: gene structure and mutation causing X-linked sideroblastic anemia with ataxia with disruption of cytosolic iron-sulfur protein maturation."

(PMID: 11050011)

[3].

"Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A)."

(PMID: 10196363)

[4].

"Isolation and chromosomal mapping of a novel ATP-binding cassette transporter conserved in mouse and human."

(PMID: 9143506)

[5].

"X-linked sideroblastic anemia and ataxia: a new family with identification of a fourth ABCB7 gene mutation."

(PMID: 22398176)

[6].

"Association study between single-nucleotide polymorphisms in 199 drug-related genes and commonly measured quantitative traits of 752 healthy Japanese subjects."

(PMID: 19343046)

[7].

"The role of the iron transporter ABCB7 in refractory anemia with ring sideroblasts."

(PMID: 18398482)

[8].

"The DNA sequence of the human X chromosome."

(PMID: 15772651)

[9].

"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

(PMID: 15489334)

[10].

"Involvement of ABC7 in the biosynthesis of heme in erythroid cells: interaction of ABC7 with ferrochelatase."