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Rabbit Anti-HDHD2B/FITC Conjugated antibody
background:
LHPP, also known as HDHD2B, is a 270 amino acid protein that exists as a homodimer and is a member of the HAD-like hydrolase superfamily. Expressed in liver, kidney and moderately in brain, LHPP is encoded by a gene located on 10, which houses over 1,200 genes and comprises nearly 4.5% of the human genome. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
Function:
Phosphatase that hydrolyzes imidodiphosphate, 3-phosphohistidine and 6-phospholysine. Has broad substrate specificity and can also hydrolyze inorganic diphosphate, but with lower efficiency (By similarity).
Subunit:
Homodimer.
Subcellular Location:
Cytoplasm. Nucleus.
Tissue Specificity:
Expressed in brain, and at lower levels in liver and kidney. Detected in thyroid (at protein level). Expressed in liver, kidney and moderately in brain.
Similarity:
Belongs to the HAD-like hydrolase superfamily.
Database links:
Entrez Gene: 12877 Human
Entrez Gene: 76429 Mouse
Entrez Gene: 361663 Rat
SwissProt: Q9H008 Human
SwissProt: Q9D7I5 Mouse
SwissProt: Q5I0D5 Rat
Unigene: 527748 Human
Unigene: 276721 Mouse
Unigene: 15275 Rat
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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