Cell Biology Antibodies 15

Anti-NSUN5 Antibody (CAB5992)

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SKU:
CAB5992
Product Type:
Antibody
Reactivity:
Human
Reactivity:
Mouse
Reactivity:
Rat
Host Species:
Rabbit
Isotype:
IgG
Antibody Type:
Polyclonal Antibody
Research Area:
Cell Biology

Description

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Antibody Name:Anti-NSUN5 Antibody
Antibody SKU:CAB5992
Antibody Size:20uL, 50uL, 100uL
Application:WB IHC
Reactivity:Human, Mouse, Rat
Host Species:Rabbit
Immunogen:Recombinant fusion protein containing a sequence corresponding to amino acids 277-466 of human NSUN5 (NP_683759.1).
Application:WB IHC
Recommended Dilution:WB 1:200 - 1:2000 IHC 1:50 - 1:200
Reactivity:Human, Mouse, Rat
Positive Samples:HepG2, RD, Rat brain
Immunogen:Recombinant fusion protein containing a sequence corresponding to amino acids 277-466 of human NSUN5 (NP_683759.1).
Purification Method:Affinity purification
Storage Buffer:Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Isotype:IgG
Sequence:SCCE LAEE DFLA VSPS DPRY HEVH YILL DPSC SGSG MPSR QLEE PGAG TPSP VRLH ALAG FQQR ALCH ALTF PSLQ RLVY STCS LCQE ENED VVRD ALQQ NPGA FRLA PALP AWPH RGLS TFPG AEHC LRAS PETT LSSG FFVA VIER VEVP SSAS QAKA SAPE RTPS PAPK RKKR QQRA AAGA CTPP CT
Gene ID:55695
Uniprot:Q96P11
Cellular Location:
Calculated MW:36kDa/42kDa/46kDa/50kDa/51kDa
Observed MW:47kDa
Synonyms:NSUN5, NOL1, NOL1R, NSUN5A, WBSCR20, WBSCR20A, p120, p120(NOL1)
Background: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.
UniProt Protein Function:S-adenosyl-L-methionine-dependent methyltransferase that specifically methylates the C5 position of cytosine 3782 in 28S rRNA.
NCBI Summary: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]
UniProt Code:Q96P11
NCBI GenInfo Identifier:270288816
NCBI Gene ID:55695
NCBI Accession:NP_001161819.1
UniProt Related Accession:Q96P11
Molecular Weight:
NCBI Full Name:probable 28S rRNA (cytosine-C(5))-methyltransferase isoform 3
NCBI Synonym Full Names:NOP2/Sun RNA methyltransferase 5
NCBI Official Symbol:NSUN5  
NCBI Official Synonym Symbols:NOL1; p120; NOL1R; NSUN5A; WBSCR20; WBSCR20A; p120(NOL1)  
NCBI Protein Information:probable 28S rRNA (cytosine-C(5))-methyltransferase
UniProt Protein Name:Probable 28S rRNA (cytosine-C(5))-methyltransferase
UniProt Synonym Protein Names:NOL1-related protein; NOL1R; NOL1/NOP2/Sun domain family member 5; Williams-Beuren syndrome chromosomal region 20A protein
UniProt Gene Name:NSUN5  
Anti-NSUN5 Antibody (CAB5992)Western blot - NSUN5 Rabbit pAb (CAB5992)
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