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RLBP1 Antibody (monoclonal) (M01)

Mouse monoclonal antibody raised against a full length recombinant RLBP1.

  • WB - RLBP1 Antibody (monoclonal) (M01) AT3649a
    Antibody Reactive Against Recombinant Protein.Western Blot detection against Immunogen (60.61 KDa) .
  • E - RLBP1 Antibody (monoclonal) (M01) AT3649a
    Detection limit for recombinant GST tagged RLBP1 is approximately 0.3ng/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 P12271
Other Accession BC004199
Reactivity Human
Host mouse
Clonality Monoclonal
Isotype IgG2a Kappa
Clone Names 1H7
Calculated MW 36474 Da
Additional Information
Gene ID 6017
Other Names Retinaldehyde-binding protein 1, Cellular retinaldehyde-binding protein, RLBP1, CRALBP
Target/Specificity RLBP1 (AAH04199, 1 a.a. ~ 317 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.
PrecautionsRLBP1 Antibody (monoclonal) (M01) is for research use only and not for use in diagnostic or therapeutic procedures.
Research Areas
Citations (0)

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The protein encoded by this gene is a 36-kD water-soluble protein which carries 11-cis-retinaldehyde or 11-cis-retinal as physiologic ligands. It may be a functional component of the visual cycle. Mutations of this gene have been associated with severe rod-cone dystrophy, Bothnia dystrophy (nonsyndromic autosomal recessive retinitis pigmentosa) and retinitis punctata albescens.


Central retinal findings in Bothnia dystrophy caused by RLBP1 sequence variation. Burstedt MS, et al. Arch Ophthalmol, 2010 Aug. PMID 20696998.Development of a Diagnostic Genetic Test for Simplex and Autosomal Recessive Retinitis Pigmentosa. Clark GR, et al. Ophthalmology, 2010 Jun 28. PMID 20591486.Bothnia dystrophy is caused by domino-like rearrangements in cellular retinaldehyde-binding protein mutant R234W. He X, et al. Proc Natl Acad Sci U S A, 2009 Nov 3. PMID 19846785.Prefrontal cortex shotgun proteome analysis reveals altered calcium homeostasis and immune system imbalance in schizophrenia. Martins-de-Souza D, et al. Eur Arch Psychiatry Clin Neurosci, 2009 Apr. PMID 19165527.Carrier of R14W in carbonic anhydrase IV presents Bothnia dystrophy phenotype caused by two allelic mutations in RLBP1. K?hn L, et al. Invest Ophthalmol Vis Sci, 2008 Jul. PMID 18344446.

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$ 315.00
Cat# AT3649a
(40 western blots)
Availability: 7-10 days
Bulk Size
Seasonal Special on Bulk Order
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