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Product Name
Alpha B Crystallin antibody
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Description
Alpha B Crystallin Rabbit Polyclonal antibody. Positive IHC detected in human eye tissue. Positive WB detected in human heart tissue, mouse heart tissue, mouse skeletal muscle tissue. Positive IP detected in mouse heart tissue. Observed molecular weight by Western-blot: 20-22 kDa
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Tested applications
ELISA, WB, IHC, IP
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Species reactivity
Human,Mouse,Rat; other species not tested.
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Alternative names
Alpha B Crystallin antibody; Alpha crystallin B chain antibody; Alpha(B) crystallin antibody; CRYA2 antibody; CRYAB antibody; crystallin antibody; alpha B antibody; CTPP2 antibody; Heat shOCk protein beta 5 antibody; HSPB5 antibody; Rosenthal fiber component antibody
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Isotype
Rabbit IgG
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Preparation
This antibody was obtained by immunization of Alpha B Crystallin recombinant protein (Accession Number: NM_001368245). Purification method: Antigen affinity purified.
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Clonality
Polyclonal
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Formulation
PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
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Storage instructions
Store at -20℃. DO NOT ALIQUOT
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Applications
Recommended Dilution:
WB: 1:500-1:5000
IP: 1:200-1:2000
IHC: 1:20-1:200
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Validations
human heart tissue were subjected to SDS PAGE followed by western blot with Catalog No:107868(CRYAB antibody) at dilution of 1:500
Immunohistochemical of paraffin-embedded human eye using Catalog No:107868(CRYAB antibody) at dilution of 1:100 (under 10x lens)
Immunohistochemical of paraffin-embedded human eye using Catalog No:107868(CRYAB antibody) at dilution of 1:100 (under 40x lens)
IP Result of anti-aB-Crystallin (IP:Catalog No:107868, 3ug; Detection:Catalog No:107868 1:500) with mouse heart tissue lysate 4000ug.
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Background
Alpha B-crystallin, encoded by CRYAB gene, is multifunctional, serving as both a major structural protein in the lens and a small heat-shock protein in other tissues in mammals. Alpha B-crystallin may contribute to the transparency and refractive index of the lens. Single nucleotide polymorphisms (SNPs) in the promoter region of CRYAB gene have been associated with in multiple sclerosis. Mutations in the CRYAB gene cause distinct clinical phenotypes including isolated posterior polar cataract, myofibrillar myopathy, cardiomyopathy, or a multisystemic disorder combining all these features. Impairment of alpha-B crystallin dimerization may be relevant to the pathogenesis of these disorders.
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Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"