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>   home   >   Products   >   Primary Antibodies   >   Signal Transduction   >   CABP4 Antibody (monoclonal) (M02)   

CABP4 Antibody (monoclonal) (M02)

Mouse monoclonal antibody raised against a full length recombinant CABP4.

  • WB - CABP4 Antibody (monoclonal) (M02) AT1363a
    Antibody Reactive Against Recombinant Protein.Western Blot detection against Immunogen (44.44 KDa) .
  • WB - CABP4 Antibody (monoclonal) (M02) AT1363a
    Western Blot analysis of CABP4 expression in transfected 293T cell line by CABP4 monoclonal antibody (M02), clone 5G11.

    Lane 1: CABP4 transfected lysate(19.6 KDa).
    Lane 2: Non-transfected lysate.
  • E - CABP4 Antibody (monoclonal) (M02) AT1363a
    Detection limit for recombinant GST tagged CABP4 is 0.3 ng/ml as a capture antibody.
Product Information
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
Primary Accession P57796
Other Accession BC033167
Reactivity Human
Host mouse
Clonality Monoclonal
Isotype IgG2b Kappa
Clone Names 5G11
Calculated MW 30433 Da
Additional Information
Gene ID 57010
Other Names Calcium-binding protein 4, CaBP4, CABP4
Target/Specificity CABP4 (AAH33167, 1 a.a. ~ 170 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
Dilution WB~~1:500~1000
Format Clear, colorless solution in phosphate buffered saline, pH 7.2 .
StorageStore at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
PrecautionsCABP4 Antibody (monoclonal) (M02) is for research use only and not for use in diagnostic or therapeutic procedures.
Research Areas
Citations (0)

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This gene encodes a member of the CABP family of calcium binding protein characterized by four EF-hand motifs. Mutations in this gene are associated with congenital stationary night blindness type 2B.


A null mutation in CABP4 causes Leber's congenital amaurosis-like phenotype. Aldahmesh MA, et al. Mol Vis, 2010 Feb 10. PMID 20157620.A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorder. Littink KW, et al. Invest Ophthalmol Vis Sci, 2009 May. PMID 19074807.Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness. Zeitz C, et al. Am J Hum Genet, 2006 Oct. PMID 16960802.Human chromosome 11 DNA sequence and analysis including novel gene identification. Taylor TD, et al. Nature, 2006 Mar 23. PMID 16554811.The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). Gerhard DS, et al. Genome Res, 2004 Oct. PMID 15489334.

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$ 315.00
Cat# AT1363a
(40 western blots)
Availability: 7-10 days
Bulk Size
Seasonal Special on Bulk Order
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