catalog number :
MBS8245298
products full name :
Anti-SETD5 Antibody
products short name :
[SETD5]
products name syn :
[KIAA1757; SET domain-containing protein 5]
other names :
[SET domain-containing protein 5 isoform 1; SET domain-containing protein 5; SET domain-containing protein 5; SET domain containing 5]
products gene name :
[SETD5]
other gene names :
[SETD5; SETD5; KIAA1757]
uniprot entry name :
SETD5_HUMAN
specificity :
Recognizes endogenous levels of SETD5 protein.
purity :
The antibody was purified by immunogen affinity chromatography.
form :
Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
storage stability :
Shipped at 4°C. Upon delivery aliquot and store at -20°C for one year. Avoid freeze/thaw cycles.
tested application :
WB, IH, IF/IC
app notes :
WB: 1/500 - 1/2000. IHC: 1/50 - 1/200. IF/IC: 1/50 - 1/100
image1 heading :
Western Blot (WB)
image2 heading :
Immunohistochemistry (IHC)
image3 heading :
Immunofluorescence (IF)
other info1 :
Immunogen: Recombinant full length protein of human SETD5
products description :
Rabbit polyclonal antibody to SETD5
ncbi acc num :
NP_001073986.1
ncbi gb acc num :
NM_001080517.2
ncbi summary :
This function of this gene has yet to be determined but mutations in this gene have been associated with autosomal dominant mental retardation-23. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2014]
uniprot summary :
SETD5: 3 isoforms of the human protein are produced by alternative splicing. Protein type: Methyltransferase, protein lysine, predicted; Methyltransferase. Chromosomal Location of Human Ortholog: 3p25.3. Molecular Function: protein binding. Disease: Mental Retardation, Autosomal Dominant 23