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>   首页   >   产品   >   一抗   >   癌症   >   MTMR14 Antibody (N-term)   

MTMR14 Antibody (N-term) 精选

Affinity Purified Rabbit Polyclonal Antibody (Pab)

     
  • 1 - MTMR14 Antibody (N-term) AP17472a
    MTMR14 Antibody (N-term) (Cat. #AP17472a) western blot analysis in Hela cell line lysates (35ug/lane).This demonstrates the MTMR14 antibody detected the MTMR14 protein (arrow).
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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, E
Primary Accession Q8NCE2
Other Accession Q8VEL2, NP_001070993.1, NP_001070994.1
Reactivity Human
Predicted Mouse, Rat, Bovine, Canine, Rabbit, Chicken
Host Rabbit
Clonality Polyclonal
Isotype Rabbit IgG
Antigen Region 18-45 aa
Additional Information
Other Names Myotubularin-related protein 14, 313-, HCV NS5A-transactivated protein 4 splice variant A-binding protein 1, NS5ATP4ABP1, hJumpy, MTMR14, C3orf29
Target/Specificity This MTMR14 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 18-45 amino acids from the N-terminal region of human MTMR14.
Dilution WB~~1:1000
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.
PrecautionsMTMR14 Antibody (N-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
Research Areas

BACKGROUND

This gene encodes a myotubularin-related protein. The encoded protein is a phosphoinositide phosphatase that specifically dephosphorylates phosphatidylinositol 3,5-biphosphate and phosphatidylinositol 3-phosphate. Mutations in this gene are correlated with autosomal dominant centronuclear myopathy. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 18.

REFERENCES

Gibbs, E.M., et al. Autophagy 6(6):819-820(2010)
Rose, J.E., et al. Mol. Med. 16 (7-8), 247-253 (2010) :
Vergne, I., et al. EMBO J. 28(15):2244-2258(2009)
Tosch, V., et al. Hum. Mol. Genet. 15(21):3098-3106(2006)

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