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SPG11, Blocking Peptide

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產(chǎn)品名稱: SPG11, Blocking Peptide
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SPG11, Blocking Peptide


SPG11, Blocking Peptide  的詳細介紹
Product Name

SPG11, Blocking Peptide

Full Product Name

SPG11 Peptide

Product Synonym Names
KIAA1840; KIAA1840; Spatacsin; Colorectal carcinoma-associated protein; spastic paraplegia 11 (autosomal recessive)
Product Gene Name

SPG11 blocking peptide

[Similar Products]
Antibody/Peptide Pairs
SPG11 peptide (MBS152232) is used for blocking the activity of SPG11 antibody (MBS150871)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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OMIM
phenotype 610844
3D Structure
ModBase 3D Structure for Q96JI7
Form/Format
Liquid
Concentration
200 ug/mL (lot specific)
Species
Human
Buffer
PBS pH 7.2 (10 mM NaH2PO4, 10 mM Na2HPO4, 130 mM NaCl) containing 0.1% bovine serum albumin and 0.02% sodium azide
Location
15 amino acids near the carboxy terminus of human SPG11.
Preparation and Storage
Store SPG11 peptide at -20 degree C, stable for one year.
Other Notes
Small volumes of SPG11 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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Applications Tested/Suitable for SPG11 blocking peptide
Blocking (BL)
Application Notes for SPG11 blocking peptide
SPG11 peptide is used for blocking the activity of SPG11 antibody.
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NCBI/Uniprot data below describe general gene information for SPG11. It may not necessarily be applicable to this product.
NCBI GI #
158253417
NCBI GeneID
80208
NCBI Accession #
AAI53880 [Other Products]
UniProt Primary Accession #
Q96JI7 [Other Products]
UniProt Secondary Accession #
Q4VC11; Q58G86; Q69YG6; Q6NW01; Q8N270; Q8TBU9; Q9H734; A8KAX9; B9EK60; F5H3N6[Other Products]
UniProt Related Accession #
Q96JI7[Other Products]
Molecular Weight
266,643 Da
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NCBI Official Full Name
Spastic paraplegia 11 (autosomal recessive)
NCBI Official Synonym Full Names
spastic paraplegia 11 (autosomal recessive)
NCBI Official Symbol
SPG11??[Similar Products]
NCBI Official Synonym Symbols
KIAA1840
??[Similar Products]
NCBI Protein Information
spatacsin; spastic paraplegia 11 protein; colorectal carcinoma-associated protein
UniProt Protein Name
Spatacsin
UniProt Synonym Protein Names
Colorectal carcinoma-associated protein; Spastic paraplegia 11 protein
Protein Family
Spatacsin
UniProt Gene Name
SPG11??[Similar Products]
UniProt Synonym Gene Names
KIAA1840??[Similar Products]
UniProt Entry Name
SPTCS_HUMAN
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NCBI Summary for SPG11
The protein encoded by this gene is a potential transmembrane protein that is phosphorylated upon DNA damage. Defects in this gene are a cause of spastic paraplegia type 11 (SPG11). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]
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UniProt Comments for SPG11
SPG11: Defects in SPG11 are the cause of spastic paraplegia autosomal recessive type 11 (SPG11). Spastic paraplegia is a neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. Rate of progression and the severity of symptoms are quite variable. Initial symptoms may include difficulty with balance, weakness and stiffness in the legs, muscle spasms, and dragging the toes when walking. In some forms of the disorder, bladder symptoms (such as incontinence) may appear, or the weakness and stiffness may spread to other parts of the body. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: Membrane protein, multi-pass; Membrane protein, integral

Chromosomal Location of Human Ortholog: 15q14

Cellular Component: lysosomal membrane; cytoplasm; nucleolus; plasma membrane; integral to membrane; cytoplasmic vesicle; cytosol

Molecular Function: protein binding

Disease: Spastic Paraplegia 11, Autosomal Recessive
Research Articles on SPG11
1. widespread accumulation of spatacsin observed in pathologic alpha-synuclein-containing inclusions suggests that spatacsin may be involved in the pathogenesis of alpha-synucleinopathies
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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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