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>   首页   >   产品   >   一抗   >   细胞生物学   >   NEU4 Antibody (C-term)   

NEU4 Antibody (C-term) 精选

Affinity Purified Rabbit Polyclonal Antibody (Pab)

     
  • 1 - NEU4 Antibody (C-term) AP10385b
    NEU4 Antibody (C-term) (Cat. #AP10385b) western blot analysis in mouse liver tissue lysates (35ug/lane).This demonstrates the NEU4 antibody detected the NEU4 protein (arrow).
  • 14 - NEU4 Antibody (C-term) AP10385b
    NEU4 antibody (C-term) (Cat. #AP10385b) immunohistochemistry analysis in formalin fixed and paraffin embedded human hepatocarcinoma followed by peroxidase conjugation of the secondary antibody and DAB staining. This data demonstrates the use of the NEU4 antibody (C-term) for immunohistochemistry. Clinical relevance has not been evaluated.
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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, IHC-P, E
Primary Accession Q8WWR8
Other Accession NP_001161072.1, NP_542779.2, NP_001161074.1, NP_001161071.1, NP_001161073.1
Reactivity Human, Mouse
Predicted Bovine, Canine
Host Rabbit
Clonality Polyclonal
Isotype Rabbit IgG
Calculated MW 51572 Da
Antigen Region 423-452 aa
Additional Information
Gene ID 129807
Other Names Sialidase-4, N-acetyl-alpha-neuraminidase 4, NEU4
Target/Specificity This NEU4 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 423-452 amino acids from the C-terminal region of human NEU4.
Dilution WB~~1:1000
IHC-P~~1:100~500
E~~Use at an assay dependent concentration.
Format Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
PrecautionsNEU4 Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures.

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

Protein Information
Name NEU4 (HGNC:21328)
Function Exo-alpha-sialidase that catalyzes the hydrolytic cleavage of the terminal sialic acid (N-acetylneuraminic acid, Neu5Ac) of a glycan moiety in the catabolism of glycolipids, glycoproteins and oligosaccharides. Efficiently hydrolyzes gangliosides including alpha- (2->3)-sialylated GD1a and GM3 and alpha-(2->8)-sialylated GD3 (PubMed:15213228, PubMed:15847605, PubMed:21521691). Hydrolyzes poly- alpha-(2->8)-sialylated neural cell adhesion molecule NCAM1 likely at growth cones, suppressing neurite outgrowth in hippocampal neurons (By similarity). May desialylate sialyl Lewis A and X antigens at the cell surface, down-regulating these glycan epitopes recognized by SELE/E selectin in the initiation of cell adhesion and extravasation (PubMed:21521691). Has sialidase activity toward mucin, fetuin and sialyllactose (PubMed:15847605).
Cellular Location [Isoform 1]: Cell membrane; Peripheral membrane protein. Endoplasmic reticulum membrane; Peripheral membrane protein. Microsome membrane; Peripheral membrane protein. Mitochondrion membrane; Peripheral membrane protein. Cell projection, neuron projection {ECO:0000250|UniProtKB:Q8BZL1} Note=Predominantly associates with endoplasmic reticulum membranes Only a small fraction associates with mitochondrial and plasma membranes.
Tissue Location [Isoform 1]: Predominant form in liver. Also expressed in brain, kidney and colon.
Research Areas

BACKGROUND

The protein encoded by this gene belongs to a family of glycohydrolytic enzymes, which remove terminal sialic acid residues from various sialo derivatives, such as glycoproteins, glycolipids, oligosaccharides, and gangliosides. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.

REFERENCES

Bigi, A., et al. Glycobiology 20(2):148-157(2010)
Xin, X., et al. Genome Res. 19(7):1262-1269(2009)
Miyagi, T., et al. Proteomics 8(16):3303-3311(2008)
Stamatos, N.M., et al. FEBS J. 272(10):2545-2556(2005)
Hillier, L.W., et al. Nature 434(7034):724-731(2005)

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