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NSUN5 Rabbit pAb

NSUN5 Rabbit pAb

     
  • 1 - NSUN5 Rabbit pAb AP57538
    Protein: U251(human)cell lyates at 40ug;
    Primary: Rabbit Anti-NSUN5 (AP57538) at 1:300;
    Secondary: 800CW Conjugated Goat (polyclonal) Anti-Rabbit IgG(H+L) at 1: 10000;
    Predicted band size:47 kD
    Observed band size:47 kD
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB
Primary Accession Q96P11
Reactivity Human
Host Rabbit
Clonality Polyclonal
Calculated MW 46692 Da
Physical State Liquid
Immunogen KLH conjugated synthetic peptide derived from human NSUN5
Epitope Specificity 2-100/429
Isotype IgG
Purity affinity purified by Protein A
Buffer 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
DISEASE Note=NSUN5 is located in the Williams-Beuren syndrome (WBS) critical region. WBS results from a hemizygous deletion of several genes on chromosome 7q11.23, thought to arise as a consequence of unequal crossing over between highly homologous low-copy repeat sequences flanking the deleted region.
Important Note This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
Background Descriptions This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013]
Additional Information
Gene ID 55695
Other Names 28S rRNA (cytosine-C(5))-methyltransferase, 2.1.1.-, NOL1-related protein {ECO:0000312|HGNC:HGNC:16385}, NOL1R {ECO:0000312|HGNC:HGNC:16385}, NOL1/NOP2/Sun domain family member 5, Williams-Beuren syndrome chromosomal region 20A protein, NSUN5 {ECO:0000303|PubMed:23913415, ECO:0000312|HGNC:HGNC:16385}
Dilution WB=1:500-2000
StorageStore at -20 °C for one year. Avoid repeated freeze/thaw cycles. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.

For Research Use Only. Not For Use In Diagnostic Procedures.

Protein Information
Name NSUN5 {ECO:0000303|PubMed:23913415, ECO:0000312|HGNC:HGNC:16385}
Function S-adenosyl-L-methionine-dependent methyltransferase that specifically methylates the C(5) position of cytosine 3782 (m5C3782) in 28S rRNA (PubMed:23913415, PubMed:31428936, PubMed:31722427). m5C3782 promotes protein translation without affecting ribosome biogenesis and fidelity (PubMed:31428936, PubMed:31722427). Required for corpus callosum and cerebral cortex development (By similarity).
Cellular Location Nucleus, nucleolus.
Tissue Location Ubiquitous (PubMed:11978965, PubMed:12073013). Detected in placenta, heart and skeletal muscle (PubMed:11978965, PubMed:12073013).
Research Areas

BACKGROUND

This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

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