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Anti-Tartrate Resistant Acid Phosphatase Polyclonal Antibody

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Catalog No. TMAB-13383

Anti-Tartrate Resistant Acid Phosphatase Polyclonal Antibody is a Rabbit antibody targeting Tartrate Resistant Acid Phosphatase. Anti-Tartrate Resistant Acid Phosphatase Polyclonal Antibody can be used in WB.

Anti-Tartrate Resistant Acid Phosphatase Polyclonal Antibody

Anti-Tartrate Resistant Acid Phosphatase Polyclonal Antibody

😃Good
Catalog No. TMAB-13383
Anti-Tartrate Resistant Acid Phosphatase Polyclonal Antibody is a Rabbit antibody targeting Tartrate Resistant Acid Phosphatase. Anti-Tartrate Resistant Acid Phosphatase Polyclonal Antibody can be used in WB.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
50 μL$2207-10 days7-10 days
100 μL$3747-10 days7-10 days
200 μL$5297-10 days7-10 days
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction

Bioactivity
Description
Anti-Tartrate Resistant Acid Phosphatase Polyclonal Antibody is a Rabbit antibody targeting Tartrate Resistant Acid Phosphatase. Anti-Tartrate Resistant Acid Phosphatase Polyclonal Antibody can be used in WB.
Ig Type
IgG
Reactivity
Human (predicted:Mouse,Rat)
Application
Recommended Dose
WB: 1:500-2000
Antibody Type
Polyclonal
Host SpeciesRabbit
Subcellular LocalizationLysosome.
ConstructionHybridoma Polyclonal Antibody
PurificationProtein A purified
AppearanceLiquid
Formulation0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Concentration1mg/ml
Research BackgroundThis gene encodes an iron containing glycoprotein which catalyzes the conversion of orthophosphoric monoester to alcohol and orthophosphate. It is the most basic of the acid phosphatases and is the only form not inhibited by L(+)-tartrate. [provided by RefSeq, Aug 2008]
Antigen Details
Immunogen
KLH conjugated synthetic peptide: human Tartrate Resistant Acid Phosphatase
Antigen Species
Human
Gene Name
ACP5
Gene ID
Protein Name
Tartrate-resistant acid phosphatase type 5
Uniprot ID
Function
Defects in ACP5 are the cause of spondyloenchondrodysplasia with immune dysregulation (SPENCDI) [MIM:607944]. 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. Note=ACP5 inactivating mutations result in a functional excess of phosphorylated osteopontin causing deregulation of osteopontin signaling and consequential autoimmune disease.
Chemical Properties
Molecular WeightTheoretical: 34 kDa.
Stability & Storage
Stability & StorageStore at 2°C-8°C for 1 month. Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles.
TransportShipping with blue ice.

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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