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SPG15, Polyclonal Antibody

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產(chǎn)品名稱: SPG15, Polyclonal Antibody
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SPG15, Polyclonal Antibody


SPG15, Polyclonal Antibody  的詳細(xì)介紹
Product Name

SPG15 (ZFYVE26), Polyclonal Antibody

Full Product Name

SPG15 Antibody

Product Synonym Names
SPG15; SPG15; FYVE-CENT; KIAA0321; Zinc finger FYVE domain-containing protein 26; FYVE domain-containing centrosomal protein; zinc finger, FYVE domain containing 26
Product Gene Name

anti-ZFYVE26 antibody

[Similar Products]
Antibody/Peptide Pairs
SPG15 peptide (MBS152259) is used for blocking the activity of SPG15 antibody (MBS150880)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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OMIM
phenotype 612012
3D Structure
ModBase 3D Structure for Q68DK2
Clonality
Polyclonal
Isotype
IgG
Host
Rabbit
Species Reactivity
Human, Mouse, Rat
Purity/Purification
SPG15 Antibody is affinity chromatography purified via peptide column.
Form/Format
Liquid
Concentration
1 mg/mL (lot specific)
Conjugate
Unconjugated
Immunogen
SPG15 antibody was raised against a 16 amino acid synthetic peptide near the carboxy terminus of human SPG15.
Buffer
SPG15 Antibody is supplied in PBS containing 0.02% sodium azide.
Preparation and Storage
SPG15 antibody can be stored at 4 degree C for three months and -20 degree C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
Other Notes
Small volumes of anti-ZFYVE26 antibody 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
anti-ZFYVE26 antibody
SPG15 Antibody: Hereditary spastic paraplegias (HSPs) are genetically and phenotypically heterogeneous disorders.? Spastic paraplegia with thinning of the corpus callosum (ARHSP-TCC) is a relatively frequent form of complicated hereditary spastic paraplegia in which mental retardation and muscle stiffness at onset are followed by slowly progressive paraparesis and cognitive deterioration. SPG15 is the second gene known to be responsible for ARHSP-TCC in the Italian population. Mutations in this gene are associated with autosomal recessive spastic paraplegia-15. SPG15 encodes a protein containing a FYVE zinc finger binding domain which is thought to target these proteins to membrane lipids through interaction with phospholipids in the membrane. SPG15 mRNA is widely distributed in human tissues, as well as in rat embryos, suggesting a possible role for this protein during embryonic development. SPG15 co-localizes partially with endoplasmic reticulum and endosome markers, suggesting a role in intracellular trafficking. Multiple isoforms of SPG15 are known to exist.
Applications Tested/Suitable for anti-ZFYVE26 antibody
ELISA (EIA), Western Blot (WB), Immunofluorescence (IF)
Application Notes for anti-ZFYVE26 antibody
SPG15 antibody can be used for detection of SPG15 by Western blot at 0.5 - 1 mug/mL. For immunofluorescence start at 20 mug/mL.

Western Blot (WB) of anti-ZFYVE26 antibody
Western blot analysis of SPG15 in K562 cell lysate with SPG15 antibody at (A) 1 and (B) 2 μg/mL.
anti-ZFYVE26 antibody Western Blot (WB) (WB) image
Immunofluorescence (IF) of anti-ZFYVE26 antibody
Immunofluorescence of SPG15 in Mouse Heart tissue with SPG15 antibody at 20 μg/mL.
anti-ZFYVE26 antibody Immunofluorescence (IF) image
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NCBI/Uniprot data below describe general gene information for ZFYVE26. It may not necessarily be applicable to this product.
NCBI GI #
119601358
NCBI GeneID
23503
NCBI Accession #
EAW80952 [Other Products]
UniProt Primary Accession #
Q68DK2 [Other Products]
UniProt Secondary Accession #
O15035; Q68DT9; Q6AW90; Q6ZR50; Q7Z3A4; Q7Z3I1; Q8N4W7; B1B5Y3; B4E2U3[Other Products]
UniProt Related Accession #
Q68DK2[Other Products]
Molecular Weight
77,970 Da
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NCBI Official Full Name
zinc finger, FYVE domain containing 26, isoform CRA_a
NCBI Official Synonym Full Names
zinc finger, FYVE domain containing 26
NCBI Official Symbol
ZFYVE26??[Similar Products]
NCBI Official Synonym Symbols
SPG15; FYVE-CENT
??[Similar Products]
NCBI Protein Information
zinc finger FYVE domain-containing protein 26; spastizin; FYVE domain-containing centrosomal protein
UniProt Protein Name
Zinc finger FYVE domain-containing protein 26
UniProt Synonym Protein Names
FYVE domain-containing centrosomal protein; FYVE-CENT; Spastizin
Protein Family
Zinc finger FYVE domain-containing protein
UniProt Gene Name
ZFYVE26??[Similar Products]
UniProt Synonym Gene Names
KIAA0321; FYVE-CENT??[Similar Products]
UniProt Entry Name
ZFY26_HUMAN
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NCBI Summary for ZFYVE26
This gene encodes a protein which contains a FYVE zinc finger binding domain. The presence of this domain is thought to target these proteins to membrane lipids through interaction with phospholipids in the membrane. Mutations in this gene are associated with autosomal recessive spastic paraplegia-15. [provided by RefSeq, Oct 2008]
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UniProt Comments for ZFYVE26
ZFYVE26: Phosphatidylinositol 3-phosphate-binding protein required for the abcission step in cytokinesis: recruited to the midbody during cytokinesis and acts as a regulator of abcission. May also be required for efficient homologous recombination DNA double-strand break repair. Interacts with AP5Z1, AP5B1, AP5S1 and SPG11. Interacts with TTC19 and KIF13A. Strongest expression in the adrenal gland, bone marrow, ***** brain, fetal brain, lung, placenta, prostate, skeletal muscle, testis, thymus, and retina. Intermediate levels are detected in other structures, including the spinal cord. 4 isoforms of the human protein are produced by alternative splicing.

Protein type: Unknown function

Chromosomal Location of Human Ortholog: 14q24.1

Cellular Component: centrosome; lysosomal membrane; midbody

Molecular Function: protein binding; metal ion binding; phosphatidylinositol 3-phosphate binding

Biological Process: cytokinesis; double-strand break repair via homologous recombination

Disease: Spastic Paraplegia 15, Autosomal Recessive
Research Articles on ZFYVE26
1. ZFYVE26 is a key determinant of autophagosome maturation
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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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