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anti-Crystallin, gamma C (CRYGC) Antikörper

Crystallins are separated into two classes taxon-specific, or enzyme, and ubiquitous. Zusätzlich bieten wir Ihnen CRYGC Proteine (10) und und viele weitere Produktgruppen zu diesem Protein an.

Gen	GeneID	UniProt
CRYGC	24277	P02529
CRYGC	1420	P07315
CRYGC	12966	Q61597

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Top anti-CRYGC Antikörper auf antikoerper-online.de

Showing 10 out of 40 products:

Katalog Nr.	Reaktivität	Wirt	Konjugat	Applikation	Menge	Lieferzeit	Preis	Details
ABIN2774014	Rind (Kuh)	Kaninchen	Unkonjugiert	WB	100 μL	2 bis 3 Tage	$289.00	Details
ABIN2854417	Human	Kaninchen	Unkonjugiert	WB	100 μL	3 bis 4 Tage	$466.18	Details
ABIN6743634	Human	Kaninchen	Unkonjugiert	WB	100 μL	11 bis 14 Tage	$551.83	Details
ABIN1497651	Human	Maus	Unkonjugiert	WB	100 μL	11 bis 14 Tage	$522.50	Details
ABIN4903384	Human	Kaninchen	Unkonjugiert	WB	100 μL	11 bis 13 Tage	$366.77	Details
ABIN2463921	Human	Kaninchen	Unkonjugiert	ELISA, WB	100 μL	2 bis 3 Tage	$446.88	Details
ABIN630603	Human	Kaninchen	Unkonjugiert	WB	50 μg	9 bis 11 Tage	$449.29	Details
ABIN514635	Human	Maus	Unkonjugiert	ELISA, WB	200 μL	11 bis 12 Tage	$364.00	Details
ABIN1712057	Human	Kaninchen	HRP	IHC (p), WB	100 μL	14 bis 21 Tage	$428.45	Details
ABIN1708432	Human	Kaninchen	Cy7	IF (p)	100 μL	14 bis 21 Tage	$428.45	Details

Weitere Produktkategorien zu CRYGC Antikörper

Am meisten referenzierte anti-CRYGC Antikörper

Human Polyclonal CRYGC Primary Antibody für IF (p), IHC (p) - ABIN1714542 : Aoki, Ogino, Tomita, Hara, Kunisada: Disruption of Rest Leads to the Early Onset of Cataracts with the Aberrant Terminal Differentiation of Lens Fiber Cells. in PLoS ONE 2016 (PubMed)

Weitere Antikörper gegen CRYGC Interaktionspartner

Human Crystallin, gamma C (CRYGC) Interaktionspartner

Identification of a novel CRYGC exon 2 mutation in a pedigree affected with congenital cataracts
Study identified eight different mutations in CRYGC associated with autosomal dominant congenital nuclear cataracts (ADCC) in a cohort of Chinese family and shows that CRYGC mutations are responsible for 4.1% of ADCC families in the cohort. The results expand the spectrum of CRYGC mutations as well as their associated phenotypes.
We examined a cohort of Chinese patients with congenital cataracts and studied the phenotypes and genotypes. Extralenticular abnormalities, such as microcornea and ocular coloboma, can also be found in patients with congenital cataracts. The phenotype of congenital cataracts associated with macular and optic disc coloboma was reported for the first time in this study.
the G129C mutation in gammaC-crystallin, which is associated with autosomal dominant congenital nuclear cataract, perturbed the unfolding process by promoting the accumulation of two distinct aggregation-prone intermediates under mild denaturing conditions.
Exome sequencing in developmental eye disease leads to identification of causal variants in GJA8, CRYGC, PAX6 and CYP1B1.
We confirm that congenital cataract is associated with a CRYGC gene mutation.
identified a CRYAA mutation in family A and a CRYGC mutation in family B with congenital cataract
A nonsense mutation c.471G>A in CRYGC is associated with autosomal dominant congenital nuclear cataracts and microcornea in a Chinese pedigree.
Molecular modeling and spectroscopic studies indicated that the mutation impaired the tertiary structure of gamma C crystallin by modifying the H-bonding network in the C-terminal domain.
Transgenic expression of mutant CRYGC5bpd gamma-crystallin at near-physiological levels causes lens opacities and fiber cell defects, confirming the pathogenicity of this mutation.
Two novel nonsynonymous variations and four reported variations in CRYAB, CRYGC, CRYGD, and GJA8, were observed.
The T5P mutation obviously changes conformation and decreases conformational stability.
calculation of the standard free-energy by equilibrium unfolding transition in guanidine hydrochloride
In gammaD-crystallin, methylation is exclusively at Cys 110, whereas in gammaC- and gammaB-crystallins, the principal methylation site is Cys 22 with minor methylation at Cys 79
the loss of interactions of T5P mutant of the gammaC-crystallin with other crystallins may play a larger role than the protection afforded by chaperone-like activity in Coppock-like cataract.
This is the first case of phenotypic heterogeneity in the primary congenital cataract specifically associated with the R168W mutation in the CRYGC gene.
Identification of a novel nonsense mutation in CRYGC in a Chinese family with autosomal dominant congenital nuclear cataracts and microcornea.
Report a new nonsense mutation (Y56X) in CRYGD and a prev'ly reported missense mutation (R12C) in CRYAA associated with nuclear autosomal dominant congenital cataract in Brazilian families. A new polymorphism (S119S) in CRYGC was observed in one family.

Mouse (Murine) Crystallin, gamma C (CRYGC) Interaktionspartner

a 1-bp deletion in gammaC-crystallin leads to cataract.
presence of measurable interactions between MIP26 and all crystallins, with the extent of interactions decreasing from alphaA- and alphaB-crystallin to betaB2- and gammaC-crystallin.

Cow (Bovine) Crystallin, gamma C (CRYGC) Interaktionspartner

The results are consistent with the hypothesis that short-range, weak, attractive interactions between alpha- and gamma-crystallins are necessary for maximum transparency of the lens.

CRYGC Antigen-Profil

Protein Überblick

Crystallins 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. Gamma-crystallins are a homogeneous group of highly symmetrical, monomeric proteins typically lacking connecting peptides and terminal extensions. They are differentially regulated after early development. Four gamma-crystallin genes (gamma-A through gamma-D) and three pseudogenes (gamma-E, gamma-F, gamma-G) are tandemly organized in a genomic segment as a gene cluster. Whether due to aging or mutations in specific genes, gamma-crystallins have been involved in cataract formation.

Genbezeichner und Symbole assoziert mit CRYGC

crystallin, gamma C (Crygc) Antikörper
crystallin gamma C (CRYGC) Antikörper
crystallin gamma C L homeolog (crygc.L) Antikörper
crystallin, gamma C (CRYGC) Antikörper
crystallin gamma C (Crygc) Antikörper
gamma-crystallin C (LOC100069179) Antikörper

ccl Antikörper
Cryg Antikörper
Cryg-5 Antikörper
cryg3 Antikörper
CRYGC Antikörper
CTRCT2 Antikörper
Len Antikörper
MGC84008 Antikörper

Bezeichner auf Proteinebene für CRYGC

crystallin, gamma polypeptide 3 , gamma-C-crystallin , gamma-crystallin 2-1 , gamma-crystallin C , crystallin, gamma-3 , gamma-crystallin 3 , gammaC-crystallin , gamma-crystallin IIIA , crystallin, gamma C

GENE ID	SPEZIES
24277	Rattus norvegicus
1420	Homo sapiens
12966	Mus musculus
281722	Bos taurus
444574	Xenopus laevis
709553	Macaca mulatta
737363	Pan troglodytes
100126770	Canis lupus familiaris
100337641	Cavia porcellus
100354942	Oryctolagus cuniculus
100069179	Equus caballus

Ausgewählte Anbieter für anti-CRYGC (CRYGC) Antikörper

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