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ABCD4 (GeneName), ATP-binding cassette sub-family D member 4 (ProteinName), ABCD4_HUMAN.
Product Name:

Human ABCD4/ ATP-binding cassette sub-family D member 4 ELISA Kit

Cat.#:
-
Brand:
EIAab®
Regulatory Status:
Alternative:

PMP70-related protein, P70R, Peroxisomal membrane protein 1-like, PXMP1-L, Peroxisomal membrane protein 69, PMP69, PXMP1L

Detection Method:
ELISA
Specificity:
Natural and recombinant human ATP-binding cassette sub-family D member 4
Sample Type:
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Sample Data:
Research Area:
-
Human ABCD4 ELISA Kit
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Human ABCD4 ELISA Kit
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Product Datasheets


General Annotation


Sub Unit:
Homodimer or heterodimer.


Function:
May be involved in intracellular processing of vitamin B12 (cobalamin). Could play a role in the lysosomal release of vitamin B12 into the cytoplasm.


Subcellular Location:
Peroxisome membrane Multi-pass membrane protein


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

[1].
"Primary structure of human PMP69, a putative peroxisomal ABC-transporter."

[2].
"Genomic organization and chromosomal localization of the human peroxisomal membrane protein-1-like protein (PXMP1-L) gene encoding a peroxisomal ABC transporter."

[3].
"Identification of a fourth half ABC transporter in the human peroxisomal membrane."

[4].
"Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism."

[5].
"Association study between single-nucleotide polymorphisms in 199 drug-related genes and commonly measured quantitative traits of 752 healthy Japanese subjects."

[6].
"Decreased expression of ABCD4 and BG1 genes early in the pathogenesis of X-linked adrenoleukodystrophy."

[7].
"Targeting of the human adrenoleukodystrophy protein to the peroxisomal membrane by an internal region containing a highly conserved motif."

[8].
"Catalog of 605 single-nucleotide polymorphisms (SNPs) among 13 genes encoding human ATP-binding cassette transporters: ABCA4, ABCA7, ABCA8, ABCD1, ABCD3, ABCD4, ABCE1, ABCF1, ABCG1, ABCG2, ABCG4, ABCG5, and ABCG8."

[9].
"Architecture of the human interactome defines protein communities and disease networks."

[10].
"Clinical or ATPase domain mutations in ABCD4 disrupt the interaction between the vitamin B12-trafficking proteins ABCD4 and LMBD1."
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