TEL: +86 571 56623320 EMAIL: [email protected]
Product Name NAV3 Chinese Name 神经元引导蛋白3抗体 Alias KIAA0938; NAV 3; NAV3; NAV3_HUMAN; Neuron navigator 3; POMFIL1; Pore membrane and/or filament-interacting-like protein 1; Steerin 3; Steerin-3; STEERIN3; Unc 53 homolog 3; Unc-53 homolog 3; unc53H3. literatures Specific References (1) | SL12151R has been referenced in 1 publications.[IF=24.633] Yanxin Li. et al. Decoding the temporal and regional specification of microglia in the developing human brain. Cell Stem Cell. 2022 Mar;: IF ; Mouse,Human.Research Area Cell biology Neurobiology Immunogen Species Rabbit Clonality Polyclonal React Species Mouse, (predicted: Human, Rat, Chicken, Horse, Sheep, ) Applications WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.Theoretical molecular weight 255kDa Cellular localization The nucleus The cell membrane Form Liquid Concentration 1mg/ml immunogen KLH conjugated synthetic peptide derived from human NAV3: 301-400/2385 Lsotype IgG Purification affinity purified by Protein A Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. PubMed PubMed Product Detail May regulate IL2 production by T-cells. May be involved in neuron regeneration.
Function:
May regulate IL2 production by T-cells. May be involved in neuron regeneration.
Subcellular Location:
Nucleus outer membrane.
Tissue Specificity:
Highly expressed in brain. Expressed at low levels in heart and placenta. Present in activated T-cells but not in resting T-cells (at protein level). Down-regulated in primary neuroblastoma.
DISEASE:
Note=A chromosomal aberration disrupting NAV3 has been found in patients with Sezary syndrome. Translocation t(12;18)(q21;q21.2).
Similarity:
Sequence similarities; Belongs to the Nav/unc-53 family.
Contains 1 CH (calponin-homology) domain.
SWISS:
Q8IVL0
Gene ID:
89795
Database links:Entrez Gene: 89795 Human
Entrez Gene: 260315 Mouse
Omim: 611629 Human
SwissProt: Q8IVL0 Human
SwissProt: Q80TN7 Mouse
Unigene: 655301 Human
Unigene: 225050 Mouse
Unigene: 394160 Mouse
Unigene: 461280 Mouse
Product Picture
Scan Wechat Qrcode