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PAPSS2, Blocking Peptide

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产品名称: PAPSS2, Blocking Peptide
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简单介绍

PAPSS2, Blocking Peptide


PAPSS2, Blocking Peptide  的详细介绍
Product Name

PAPSS2, Blocking Peptide

Full Product Name

PAPSS2 Peptide

Product Gene Name

PAPSS2 blocking peptide

[Similar Products]
Product Synonym Gene Name
ATPSK2; SK2[Similar Products]
Antibody/Peptide Pairs
PAPSS2 peptide (MBS3234066) is used for blocking the activity of PAPSS2 antibody (MBS3209103)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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OMIM
603005
3D Structure
ModBase 3D Structure for O95340
Form/Format
Lyophilized powder
Preparation and Storage
Add 100ul of sterile PBS. Final peptide concentration is 1 mg/ml in PBS. For longer periods of storage, store at -20 degree C. Avoid repeat freeze-thaw cycles.
Other Notes
Small volumes of PAPSS2 blocking peptide 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.
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Related Product Information for
PAPSS2 blocking peptide
This is a synthetic peptide designed for use in combination with anti-PAPSS2 antibody made

Target Description: Sulfation is a common modification of endogenous (lipids, proteins, and carbohydrates) and exogenous (xenobiotics and drugs) compounds. In mammals, the sulfate source is 3'-phosphoadenosine 5'-phosphosulfate (PAPS), created from ATP and inorganic sulfate. Two different tissue isoforms encoded by different genes synthesize PAPS. PAPSS2 is one of the two PAPS synthetases. Defects in this gene cause the Pakistani type of spondyloepimetaphyseal dysplasia. Two alternatively spliced transcript variants that encode different isoforms have been described for this gene.Sulfation is a common modification of endogenous (lipids, proteins, and carbohydrates) and exogenous (xenobiotics and drugs) compounds. In mammals, the sulfate source is 3'-phosphoadenosine 5'-phosphosulfate (PAPS), created from ATP and inorganic sulfate. Two different tissue isoforms encoded by different genes synthesize PAPS. This gene encodes one of the two PAPS synthetases. Defects in this gene cause the Pakistani type of spondyloepimetaphyseal dysplasia. Two alternatively spliced transcript variants that encode different isoforms have been described for this gene.
Product Categories/Family for PAPSS2 blocking peptide
Peptide
Applications Tested/Suitable for PAPSS2 blocking peptide
Immunohistochemistry (IHC), Western Blot (WB)
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NCBI/Uniprot data below describe general gene information for PAPSS2. It may not necessarily be applicable to this product.
NCBI GI #
62912492
NCBI GeneID
9060
NCBI Accession #
NP_001015880 [Other Products]
NCBI GenBank Nucleotide #
NM_001015880 [Other Products]
UniProt Primary Accession #
O95340 [Other Products]
UniProt Related Accession #
O95340[Other Products]
Molecular Weight
70kDa
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NCBI Official Full Name
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 2 isoform b
NCBI Official Synonym Full Names
3'-phosphoadenosine 5'-phosphosulfate synthase 2
NCBI Official Symbol
PAPSS2  [Similar Products]
NCBI Official Synonym Symbols
SK2; BCYM4; ATPSK2
  [Similar Products]
NCBI Protein Information
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 2
UniProt Protein Name
Bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 2
UniProt Synonym Protein Names
Sulfurylase kinase 2; SK 2; SK2
Protein Family
Bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase
UniProt Gene Name
PAPSS2  [Similar Products]
UniProt Synonym Gene Names
ATPSK2; PAPS synthase 2; PAPSS 2; SK 2; SK2; SAT  [Similar Products]
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NCBI Summary for PAPSS2
Sulfation is a common modification of endogenous (lipids, proteins, and carbohydrates) and exogenous (xenobiotics and drugs) compounds. In mammals, the sulfate source is 3'-phosphoadenosine 5'-phosphosulfate (PAPS), created from ATP and inorganic sulfate. Two different tissue isoforms encoded by different genes synthesize PAPS. This gene encodes one of the two PAPS synthetases. Defects in this gene cause the Pakistani type of spondyloepimetaphyseal dysplasia. Two alternatively spliced transcript variants that encode different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]
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UniProt Comments for PAPSS2
Bifunctional enzyme with both ATP sulfurylase and APS kinase activity, which mediates two steps in the sulfate activation pathway. The first step is the transfer of a sulfate group to ATP to yield adenosine 5'-phosphosulfate (APS), and the second step is the transfer of a phosphate group from ATP to APS yielding 3'-phosphoadenylylsulfate (PAPS: activated sulfate donor used by sulfotransferase). In mammals, PAPS is the sole source of sulfate; APS appears to be only an intermediate in the sulfate-activation pathway. May have a important role in skeletogenesis during postnatal growth ().
Research Articles on PAPSS2
1. Energy-dependent scoring of docking solutions identified the interaction as specific for the PAPSS2 and SULT2A1 isoforms
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Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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