Vergleich

CTRP6

ArtNr 18-783-75560
Hersteller GENWAY
Menge 0.1 mg
Kategorie
Typ Antibody
Applikationen WB, IHC
Specific against other
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias GWB-E643CB
Similar products 18-783-75560
Lieferbar
Genway ID:
GWB-E643CB
Gene ID:
114904
Isotype:
Ployclonal IgG.
Specificity:
CTRP6 (C-Terminal).
Immunogen:
A 15 amino acid peptide located near the carboxy-terminus of human CTRP6.
Specificity Note:
This product detects an epitope within the C-terminal (CT) region of human C1q and TNF related protein 6 (CTRP6) also known as C1QTNF6. CTRP6 is an adipokine; proteins which are thought to act mainly on liver and muscle tissue to control glucose and lipid metabolism. CTRP6 is highly post-translationally modified containing at least 4 glycosylation motifs. It has a predicted molecular weight of 29kD and an observed molecular weight of 42kD. Histology: HeLa cells.
Antiserum Preparation:
Antisera to human CTRP6 (CT) were raised by repeated immunisations of rabbits with highly purified antigen. Purified IgG prepared by affinity chromatography.
Buffer Solution:
Phosphate buffered saline
Preservative Stabilisers:
0. 02% Sodium Azide (NaN3)Suggested
Dilution:
Western Blot: This product detects a band of approximately 42kDa in heLa cell lysates. These proteins often migrate in SDS-PAGE at positions other that their predicted size. Suggested
Dilution:
Immunohistology - Frozen - 10ug/mlWestern Blotting - 1 - 2ug/ml
Subunit:
Interacts with tubulin alpha ACTN2 ANKHD1 ATF4 ATF5 CEP63 EIF3S3 MAP1A NDEL1 PAFAH1B1 RANBP9 SPTBN4 SYNE1 and TRAF3IP1. Interaction with microtubules may be mediated in part by TRAF3IP1.
Subcellular Location:
Cytoplasm. Centrosome. Note=Localizes to neurites (By similarity). Localizes to punctate cytoplasmic foci which overlap in part with mitochondria. Also localizes to the centrosome.
Tissue Specificity:
Ubiquitous. Highly expressed in the dentate gyrus of the hippocampus. Also expressed in the temporal and parahippocampal cortices and cells of the white matter. Developmental Stage: Expression rises within the dentate gyrus and temporal cortex from the neonatal period to infancy declines markedly in adolescence and declines further with aging.
Disease:
A chromosomal aberration involving DISC1 segregates with schizophrenia and related psychiatric disorders in a large Scottish family. Translocation t(1; 11)(q42. 1; q14. 3). The truncated DISC1 protein produced by this translocation is unable to interact with ATF4 ATF5 and NDEL1.
Disease:
Genetic variation in DISC1 may be associated with susceptibility to schizophrenia 9 (SCZD9) [MIM:604906]. Schizophrenia [MIM:181500] is a psychosis a disorder of thought and sense of self. Although it affects emotions it is distinguished from mood disorders in which such disturbances are primary. Similarly there may be mild impairment of cognitive function and it is distinguished from the dementias in which disturbed cognitive function is considered primary. No objective biological test for schizophrenia exists. Schizophrenia is a common disorder with a lifetime prevalence of approximately 1%. It is highly heritable but the genetics are complex.
Disease:
Genetic variation in DISC1 may be associated with susceptibility to schizoaffective disorder [MIM:181500]. Schizoaffective disorder is a psychiatric condition characterized by the co-occurrence of symptoms of both mood disorder and psychosis. 1. Chang. A. C. Y. et al. (2006) Phenotype-Based Identification of Host Genes Required for Replication of African Swine Fever Virus. 2. Holzbeierlein. J. et al. (2004) Gene Expression Analysis of Human Prostate Carcinoma during Hormonal Therapy Identifies Androgen-Responsive Genes and Mechanisms of Therapy Resistance. 3. Schaner. M. E. (2003) Gene Expression Patterns in Ovarian Carcinomas.

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Alle Produkte sind nur für Forschungszwecke bestimmt. Nicht für den menschlichen, tierärztlichen oder therapeutischen Gebrauch.

Menge: 0.1 mg
Lieferbar: In stock
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Lieferung vsl. bis 30.10.2025 

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