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AB105393

Anti-PIWIL1 antibody

4

(4 Reviews)

|

(5 Publications)

Rabbit Polyclonal PIWIL1 antibody. Suitable for WB and reacts with Human samples. Cited in 5 publications. Immunogen corresponding to Synthetic Peptide within Human PIWIL1 aa 50-150.

View Alternative Names

HIWI, PIWIL1, Piwi-like protein 1

2 Images
Western blot - Anti-PIWIL1 antibody (AB105393)
  • WB

Unknown

Western blot - Anti-PIWIL1 antibody (AB105393)

All lanes:

Western blot - Anti-PIWIL1 antibody (ab105393) at 1 µg/mL

Lane 1:

HepG2 cell lysate without blocking peptide. at 15 µg

Lane 2:

HepG2 cell lysate with blocking peptide. at 15 µg

Predicted band size: 66 kDa,98 kDa

Observed band size: 66 kDa

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Western blot - Anti-PIWIL1 antibody (AB105393)
  • WB

CiteAb

Western blot - Anti-PIWIL1 antibody (AB105393)

PIWIL1 western blot using anti-PIWIL1 antibody ab105393. Publication image and figure legend from Chen, Z., Che, Q., et al., 2015, BMC Cancer, PubMed 26506848.

ab105393 was used in this publication in western blot. This may not be the same as the application(s) guaranteed by Abcam. For a full list of applications guaranteed by Abcam for ab105393 please see the product overview.

Overexpression or knockdown of Piwil1 in human endometrial cancer cell lines. a Stable transfection of Ishikawa cells with shRNA against Piwil1 and HEC-1B cells with Piwil1 expression plasmids. The percentage of transfected cells with fluorescence was > 95 %. (b and c) RT-qPCR and western blot demonstrated expression level of Piwil1 in Ishikawa, IshikawaNT and IshikawashPiwil1 cells or HEC-1B, HEC-1BEV and HEC-1BexPiwil1 cells (*P < 0.05). d Representative immunofluorescence images showing Piwil1 expression in IshikawaNT and IshikawashPiwil1 cells or in HEC-1BEV and HEC-1BexPiwil1 cells. Nuclei were stained with DAPI. Scale bars, 25 μm

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Key facts

Host species

Rabbit

Clonality

Polyclonal

Isotype

IgG

Carrier free

No

Reacts with

Human

Applications

WB

applications

Immunogen

Synthetic Peptide within Human PIWIL1 aa 50-150. The exact immunogen used to generate this antibody is proprietary information.

Q96J94

Specificity

At least three isoforms of PIWIL1 are known to exist; ab105393 will recognize the two longest isoforms. ab105393 is predicted to not cross-react with other PIWI family members.

Reactivity data

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Properties and storage information

Form
Liquid
Purification technique
Affinity purification Immunogen
Storage buffer
pH: 7.2 Preservative: 0.02% Sodium azide Constituents: PBS
Shipped at conditions
Blue Ice
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Storage information
Avoid freeze / thaw cycle

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

PIWIL1 also known as Piwi-like protein 1 is a member of the Argonaute family with a molecular mass of approximately 97 kDa. This protein functions mechanically by binding to PIWI-interacting RNAs (piRNAs) which are small non-coding RNAs. PIWIL1 exhibits expression in germline cells specifically in testes therefore playing an important role in spermatogenesis. It facilitates the formation of piRNA complexes contributing to the regulation of gene silencing.
Biological function summary

PIWIL1 contributes to maintaining genomic integrity through its role in RNA-mediated gene regulation. It forms part of the piRNA-induced silencing complex. This complex targets transposable elements and prevents their mobility an important function for genomic stability. PIWIL1's involvement in gametogenesis highlights its essential function in reproductive biology and cellular processes where piRNA pathways operate.

Pathways

The PIWIL1 protein plays significant roles within the piRNA pathway which is important for transposon silencing and germline integrity. PIWIL1 interacts with MILI and MIWI two proteins that also participate in the silencing of transposable elements. This pathway intersects with other gene regulation pathways influencing the overall expression landscape necessary for proper cellular function in reproductive tissues.

PIWIL1 alterations have associations with germ cell tumors and fertility issues. Disruption in piRNA pathway components like PIWIL1 and its partners MIWI and MILI can lead to failures in genomic defense mechanisms influencing cancer development in germline cells. Additionally defects in PIWIL1 expression can contribute to infertility due to its role in spermatogenesis. Understanding these associations provides insights into potential diagnostic and therapeutic targets for related conditions.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Endoribonuclease that plays a central role in postnatal germ cells by repressing transposable elements and preventing their mobilization, which is essential for the germline integrity. Acts via the piRNA metabolic process, which mediates the repression of transposable elements during meiosis by forming complexes composed of piRNAs and Piwi proteins and governs the methylation and subsequent repression of transposons. Directly binds methylated piRNAs, a class of 24 to 30 nucleotide RNAs that are generated by a Dicer-independent mechanism and are primarily derived from transposons and other repeated sequence elements. Strongly prefers a uridine in the first position of their guide (g1U preference, also named 1U-bias). Not involved in the piRNA amplification loop, also named ping-pong amplification cycle. Acts as an endoribonuclease that cleaves transposon messenger RNAs. Besides their function in transposable elements repression, piRNAs are probably involved in other processes during meiosis such as translation regulation. Probable component of some RISC complex, which mediates RNA cleavage and translational silencing. Also plays a role in the formation of chromatoid bodies and is required for some miRNAs stability. Required to sequester RNF8 in the cytoplasm until late spermatogenesis; RNF8 being released upon ubiquitination and degradation of PIWIL1.. Isoform 3. May be a negative developmental regulator (PubMed : 12037681, PubMed : 16287078).
See full target information PIWIL1

Publications (5)

Recent publications for all applications. Explore the full list and refine your search

International journal of molecular sciences 24: PubMed37298298

2023

cDNA Cloning of Feline PIWIL1 and Evaluation of Expression in the Testis of the Domestic Cat.

Applications

Unspecified application

Species

Unspecified reactive species

Leanne Stalker,Alanna G Backx,Allison K Tscherner,Stewart J Russell,Robert A Foster,Jonathan LaMarre

Cell communication and signaling : CCS 18:84 PubMed32503542

2020

Estrogen-ERα signaling and DNA hypomethylation co-regulate expression of stem cell protein PIWIL1 in ERα-positive endometrial cancer cells.

Applications

Unspecified application

Species

Unspecified reactive species

Zheng Chen,Hua-Jing Yang,Qin Lin,Min-Jiao Zhu,Ying-Ying Yu,Xiao-Ying He,Xiao-Ping Wan

Scientific reports 10:8567 PubMed32444626

2020

Detrimental effects of flame retardant, PBB153, exposure on sperm and future generations.

Applications

Unspecified application

Species

Unspecified reactive species

Katherine Watkins Greeson,Kristen L Fowler,Paige M Estave,S Kate Thompson,Chelsea Wagner,R Clayton Edenfield,Krista M Symosko,Alyse N Steves,Elizabeth M Marder,Metrecia L Terrell,Hillary Barton,Michael Koval,Michele Marcus,Charles A Easley

Cells 8: PubMed31694219

2019

Molecular and Functional Characterization of the Somatic PIWIL1/piRNA Pathway in Colorectal Cancer Cells.

Applications

Unspecified application

Species

Unspecified reactive species

Assunta Sellitto,Konstantinos Geles,Ylenia D'Agostino,Marisa Conte,Elena Alexandrova,Domenico Rocco,Giovanni Nassa,Giorgio Giurato,Roberta Tarallo,Alessandro Weisz,Francesca Rizzo

BMC cancer 15:811 PubMed26506848

2015

Stem cell protein Piwil1 endowed endometrial cancer cells with stem-like properties via inducing epithelial-mesenchymal transition.

Applications

IHC

Species

Unspecified reactive species

Zheng Chen,Qi Che,Xiaoying He,Fangyuan Wang,Huihui Wang,Minjiao Zhu,Jing Sun,Xiaoping Wan
View all publications

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