
Thermo Fisher Scientific NSD1 Polyclonal Antibody
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Applications
Tested Dilution
Publications
Western Blot (WB)
1:500-1:1,000
ELISA (ELISA)
1 µg/mL
Product Specifications
Species Reactivity
Human, Mouse
Host/Isotype
Rabbit / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 60-260 of human NSD1 (NP_071900.2). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
NSD1,
uniProtId:
Q96L73-1,
ncbiNodeId:
9606,
antigenRange:
60-260,
antigenLength:
2696,
antigenImageFileName:
PA5-121252_NSD1_Q96L73-1_Rabbit.svg,
antigenImageFileNamePDP:
PA5-121252_NSD1_Q96L73-1_Rabbit_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1.97 mg/mL
Purification
Affinity Chromatography
Storage buffer
PBS, pH 7.3, with 50% glycerol
Contains
0.09% sodium azide
Storage conditions
-20° C, Avoid Freeze/Thaw Cycles
Shipping conditions
Wet ice
RRID
AB_2914824
Product Specific Information
Positive test controls include: 293T, A-549, MCF7, SW480, Mouse kidney, Mouse lung. The target is usually found in the following locations: Chromosome, Nucleus.
Immunogen sequence: AYGQDSPSCY IPLRRLQDLA SMINVEYLNG SADGSESFQD PEKSDSRAQT PIVCTSLSPG GPTALAMKQE PSCNNSPELQ VKVTKTIKNG FLHFENFTCV DDADVDSEMD PEQPVTEDES IEEIFEETQT NATCNYETKS ENGVKVAMGS EQDSTPESRH GAVKSPFLPL APQTETQKNK QRNEVDGSNE KAALLPAPFS L
Target Information
This gene encodes a protein containing a SET domain, 2 LXXLL motifs, 3 nuclear translocation signals (NLSs), 4 plant homeodomain (PHD) finger regions, and a proline-rich region. The encoded protein enhances androgen receptor (AR) transactivation, and this enhancement can be increased further in the presence of other androgen receptor associated coregulators. This protein may act as a nucleus-localized, basic transcriptional factor and also as a bifunctional transcriptional regulator. Mutations of this gene have been associated with Sotos syndrome and Weaver syndrome. One version of childhood acute myeloid leukemia is the result of a cryptic translocation with the breakpoints occurring within nuclear receptor-binding Su-var, enhancer of zeste, and trithorax domain protein 1 on chromosome 5 and nucleoporin, 98-kd on chromosome 11. Two transcript variants encoding distinct isoforms have been identified for this gene.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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