CRBB3 rabbit pAb

CRBB3 rabbit pAb

AO-06-ES17232-100

CRBB3 rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES17232
Product nameCRBB3 rabbit pAb
ReactivityHuman; Mouse;Rat
ApplicationsWB
Other name
Size100μL
Unit price ($)248
Human gene ID1417
Human Swiss-ProtP26998
SourceRabbit
IsotypeIgG
TargetCRBB3
Fields
Gene nameCRYBB3 CRYB3
Protein nameCRBB3
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID12962
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ9JJU9
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID64349
Rat gene linkView Rat Gene
Rat Swiss-ProtP02524
Rat Swiss linkView Rat Swiss-Prot
ImmunogenSynthesized peptide derived from human CRBB3 AA range: 110-160
SpecificityThis antibody detects endogenous levels of CRBB3 at Human/Mouse/Rat
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000
PurificationThe antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)23kD
Observed band (KD)
BackgroundCrystallins are separated into two classes: taxon-specific, or enzyme, and ubiquitous. The latter class constitutes the major proteins of vertebrate eye lens and maintains the transparency and refractive index of the lens. Since lens central fiber cells lose their nuclei during development, these crystallins are made and then retained throughout life, making them extremely stable proteins. Mammalian lens crystallins are divided into alpha, beta, and gamma families; beta and gamma crystallins are also considered as a superfamily. Alpha and beta families are further divided into acidic and basic groups. Seven protein regions exist in crystallins: four homologous motifs, a connecting peptide, and N- and C-terminal extensions. Beta-crystallins, the most heterogeneous, differ by the presence of the C-terminal extension (present in the basic group, none in the acidic group). Beta-crystallins form aggregates of different sizes and are able to self-associate to form dimers or to form heterodimers with other beta-crystallins. This gene, a beta basic group member, is part of a gene cluster with beta-A4, beta-B1, and beta-B2. Mutations in this gene result in cataract congenital nuclear autosomal recessive type 2. [provided by RefSeq, Feb 2013],
Functiondisease:Crystallins do not turn over as the lens ages, providing ample opportunity for post-translational modifications or oxidations. These modifications may change crystallin solubility properties and favor senile cataract.,disease:Defects in CRYBB3 are the cause of autosomal recessive congenital nuclear cataract 2 (CATCN2) [MIM:609741]. CATCN2 is a form of non-syndromic congenital cataract. Non-syndromic congenital cataracts vary markedly in severity and morphology, affecting the nuclear, cortical, polar, or subcapsular parts of the lens or, in severe cases, the entire lens, with a variety of types of opacity. They are one of the major causes of vision loss in children worldwide and are responsible for approximately one third of blindness in infants. Congenital cataracts can lead to permanent blindness by interfering with the sharp focus of light on the retina during critical developm
Subcellular location
Expression

Additional Images

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Western blot analysis of lysates from MCF-7 cells, primary antibody was diluted at 1:1000, 4°over night
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: AO-06-ES17232-100
: 10 Items
Hurry! only 10 items left in stock.

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