Product Name
ACP5 / TRAP, Recombinant Protein
Full Product Name
Recombinant Mouse ACP5 / TRAP Protein (His tag)
Product Synonym Names
TRACP, TRAP, Acp5
Product Gene Name
ACP5 / TRAP recombinant protein
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for Q05117
Purity/Purification
> 95 % as determined by SDS-PAGE
Form/Format
Lyophilized from sterile PBS, pH 7.4
Predicted N Terminal
Ala 23
Endotoxin
< 1.0 EU per mug of the protein as determined by the LAL method
Preparation and Storage
Samples are stable for up to twelve months from date of receipt at -70 degree C
ISO Certification
Manufactured in an ISO 9001:2015 Certified Laboratory.
Other Notes
Small volumes of ACP5 / TRAP recombinant protein vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
ACP5 / TRAP recombinant protein
Background: Tartrate-resistant acid phosphatase (TRACP) or acid phosphatase 5, tartrate resistant (ACP5 or TRAP) is a glycosylated monomeric metalloenzyme expressed in mammals. TRACP is associated with osteoblast migration to bone resorption sites, and, once there, TRACP is believed to initiate osteoblast differentiation, activation, and proliferation. TRACP once considered to be just a histochemical marker of osteoclasts is now recognised to be a molecule of widespread occurrence with functions in both the skeleton and the immune system. Two forms of TRACP circulate in human blood, TRACP 5a derived from macrophages and dendritic cells, and TRACP-5b derived from osteoclasts. Recent data have demonstrated the utility of TRACP-5b as a marker of osteoclast number and bone resorption, and serum TRACP-5a as a marker of inflammatory conditions. TRACP is expressed by osteoclasts, macrophages, dendritic cells and a number of other cell type s. It has a critical role in many
biological processes including skeletal development, collagen synthesis and degradation, the mineralisation of bone, cytokine production by macrophages and dendritic cells, macrophage recruitment, dendritic cell maturation and a role in the development of Th1 responses.
Description: A DNA sequence encoding the pro form of mouse ACP5 (NP_031414.1) (Met 1-Pro 327) was fused with a polyhistidine tag at the C-terminus.
Application Notes for ACP5 / TRAP recombinant protein
The recombinant mouse ACP5 consists of 316 amino acids and has a predicted molecular mass of 35.8 kDa as estimated in SDS-PAGE under reducing conditions.
SDS-PAGE of ACP5 / TRAP recombinant protein
NCBI/Uniprot data below describe general gene information for ACP5 / TRAP. It may not necessarily be applicable to this product.
NCBI Accession #
NP_031414.1
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NCBI GenBank Nucleotide #
NM_007388.3
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UniProt Primary Accession #
Q05117
[Other Products]
UniProt Related Accession #
Q05117[Other Products]
Molecular Weight
36,807 Da
NCBI Official Full Name
tartrate-resistant acid phosphatase type 5
NCBI Official Synonym Full Names
acid phosphatase 5, tartrate resistant
NCBI Official Symbol
Acp5 [Similar Products]
NCBI Official Synonym Symbols
TRAP; TRACP
[Similar Products]
NCBI Protein Information
tartrate-resistant acid phosphatase type 5
UniProt Protein Name
Tartrate-resistant acid phosphatase type 5
UniProt Synonym Protein Names
Tartrate-resistant acid ATPase; TrATPase; Type 5 acid phosphatase
UniProt Gene Name
Acp5 [Similar Products]
UniProt Synonym Gene Names
T5ap; Trap; TR-AP; TrATPase [Similar Products]
UniProt Comments for ACP5 / TRAP
ACP5: Involved in osteopontin/bone sialoprotein dephosphorylation. Its expression seems to increase in certain pathological states such as Gaucher and Hodgkin diseases, the hairy cell, the B-cell, and the T-cell leukemias. Defects in ACP5 are the cause of spondyloenchondrodysplasia with immune dysregulation (SPENCDI). A disease characterized by vertebral and metaphyseal dysplasia, spasticity with cerebral calcifications, and strong predisposition to autoimmune diseases. The skeletal dysplasia is characterized by radiolucent and irregular spondylar and metaphyseal lesions that represent islands of chondroid tissue within bone. ACP5 inactivating mutations result in a functional excess of phosphorylated osteopontin causing deregulation of osteopontin signaling and consequential autoimmune disease. Belongs to the metallophosphoesterase superfamily. Purple acid phosphatase family.
Protein type: Cofactor and Vitamin Metabolism - riboflavin; EC 3.1.3.2; Motility/polarity/chemotaxis; Phosphatase
Chromosomal Location of Human Ortholog: 9 A3|9 8.38 cM
Cellular Component: lysosome
Molecular Function: acid phosphatase activity
Biological Process: bone resorption; defense response to Gram-positive bacterium; dephosphorylation; negative regulation of inflammatory response; negative regulation of interleukin-1 beta production; negative regulation of interleukin-12 production; negative regulation of nitric oxide biosynthetic process; negative regulation of superoxide release; negative regulation of tumor necrosis factor production; response to cytokine stimulus; response to lipopolysaccharide
Research Articles on ACP5 / TRAP
1. Uteroferrin is a cytokine secreted by uterine glands in response to progesterone that promotes fetal erythropoiesis at various stages of pregnancy.
Precautions
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Disclaimer
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