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AB164675

Recombinant Human KLHL22 protein (GST tag N-Terminus)

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Recombinant Human KLHL22 protein (GST tag N-Terminus) is a Human Full Length protein, in the 1 to 634 aa range, expressed in Wheat germ, suitable for ELISA, WB.

View Alternative Names

Kelch-like protein 22, KLHL22

1 Images
SDS-PAGE - Recombinant Human KLHL22 protein (GST tag N-Terminus) (AB164675)
  • SDS-PAGE

Supplier Data

SDS-PAGE - Recombinant Human KLHL22 protein (GST tag N-Terminus) (AB164675)

ab164675 on a 12.5% SDS-PAGE stained with Coomassie Blue.

Key facts

Expression system

Wheat germ

Tags

GST tag N-Terminus

Applications

ELISA, WB

applications

Biologically active

No

Accession

Q53GT1

Animal free

No

Carrier free

No

Species

Human

Storage buffer

pH: 8 Constituents: 0.79% Tris HCl, 0.31% Glutathione

storage-buffer

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Reactivity", "Dilution Info", "Notes"] }, "values": { "ELISA": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" }, "WB": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" } } }

Sequence info

[{"sequence":"MAEEQEFTQLCKLPAQPSHPHCVNNTYRSAQHSQALLRGLLALRDSGILFDVVLVVEGRHIEAHRILLAASCDYFRGMFAGGLKEMEQEEVLIHGVSYNAMCQILHFIYTSELELSLSNVQETLVAACQLQIPEIIHFCCDFLMSWVDEENILDVYRLAELFDLSRLTEQLDTYILKNFVAFSRTDKYRQLPLEKVYSLLSSNRLEVSCETEVYEGALLYHYSLEQVQADQISLHEPPKLLETVRFPLMEAEVLQRLHDKLDPSPLRDTVASALMYHRNESLQPSLQSPQTELRSDFQCVVGFGGIHSTPSTVLSDQAKYLNPLLGEWKHFTASLAPRMSNQGIAVLNNFVYLIGGDNNVQGFRAESRCWRYDPRHNRWFQIQSLQQEHADLSVCVVGRYIYAVAGRDYHNDLNAVERYDPATNSWAYVAPLKREVYAHAGATLEGKMYITCGRRGEDYLKETHCYDPGSNTWHTLADGPVRRAWHGMATLLNKLYVIGGSNNDAGYRRDVHQVACYSCTSGQWSSVCPLPAGHGEPGIAVLDNRIYVLGGRSHNRGSRTGYVHIYDVEKDCWEEGPQLDNSISGLAACVLTLPRSLLLEPPRGTPDRSQADPDFASEVMSVSDWEEFDNSSED","proteinLength":"Full Length","predictedMolecularWeight":null,"actualMolecularWeight":null,"aminoAcidEnd":634,"aminoAcidStart":1,"nature":"Recombinant","expressionSystem":"Wheat germ","accessionNumber":"Q53GT1","tags":[{"tag":"GST","terminus":"N-Terminus"}]}]

Properties and storage information

Shipped at conditions
Dry Ice
Appropriate short-term storage conditions
-80°C
Appropriate long-term storage conditions
-80°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle
False

Supplementary information

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

The target KLHL22 also known as kelch-like family member 22 is a protein that plays a significant role in cellular processes. KLHL22 consists of 623 amino acids and has a molecular mass of approximately 68 kDa. This protein is expressed in various tissues including the brain liver and kidney indicating its broad functional importance in the human body. KLHL22 functions as a component of a Cullin-RING E3 ubiquitin ligase complex where it facilitates the ubiquitination and subsequent degradation of specific protein substrates.
Biological function summary

KLHL22 is involved in regulating protein turnover by targeting proteins for ubiquitination influencing processes such as cell cycle progression and signal transduction. It operates as an adaptor protein within the Cullin-RING E3 ubiquitin ligase complex linking substrate proteins to the complex for ubiquitination. By regulating the degradation of key proteins KLHL22 impacts cellular homeostasis and various physiological responses demonstrating its importance in maintaining cellular order.

Pathways

KLHL22 contributes to the ubiquitin-proteasome pathway where it assists in protein degradation and turnover maintaining protein quality control. It also associates with the cell cycle regulation pathway interacting with proteins such as CUL3 within the Cullin-RING complex to ensure cell cycle progression by timely degradation of cyclins and other regulatory proteins. These pathway involvements highlight KLHL22's role in cellular regulation and proteostasis.

KLHL22 has been linked to neurological disorders and cancer. Abnormal expression or mutations in KLHL22 contribute to the development of certain neurodegenerative diseases with its disruption affecting neuronal protein homeostasis. Additionally its interaction with proteins like NRF2 is significant in cancer where altered ubiquitination regulates responses to oxidative stress. Understanding KLHL22's role in these conditions could offer insights into therapeutic targets for managing such diseases.

Specifications

Form

Liquid

General info

Function

Substrate-specific adapter of a BCR (BTB-CUL3-RBX1) E3 ubiquitin ligase complex required for chromosome alignment and localization of PLK1 at kinetochores. The BCR(KLHL22) ubiquitin ligase complex mediates monoubiquitination of PLK1, leading to PLK1 dissociation from phosphoreceptor proteins and subsequent removal from kinetochores, allowing silencing of the spindle assembly checkpoint (SAC) and chromosome segregation. Monoubiquitination of PLK1 does not lead to PLK1 degradation (PubMed : 19995937, PubMed : 23455478). The BCR(KLHL22) ubiquitin ligase complex is also responsible for the amino acid-stimulated 'Lys-48' polyubiquitination and proteasomal degradation of DEPDC5. Through the degradation of DEPDC5, releases the GATOR1 complex-mediated inhibition of the TORC1 pathway. It is therefore an amino acid-dependent activator within the amino acid-sensing branch of the TORC1 pathway, indirectly regulating different cellular processes including cell growth and autophagy (PubMed : 29769719).

Subcellular localisation

Cytoskeleton

Product protocols

Target data

Substrate-specific adapter of a BCR (BTB-CUL3-RBX1) E3 ubiquitin ligase complex required for chromosome alignment and localization of PLK1 at kinetochores. The BCR(KLHL22) ubiquitin ligase complex mediates monoubiquitination of PLK1, leading to PLK1 dissociation from phosphoreceptor proteins and subsequent removal from kinetochores, allowing silencing of the spindle assembly checkpoint (SAC) and chromosome segregation. Monoubiquitination of PLK1 does not lead to PLK1 degradation (PubMed : 19995937, PubMed : 23455478). The BCR(KLHL22) ubiquitin ligase complex is also responsible for the amino acid-stimulated 'Lys-48' polyubiquitination and proteasomal degradation of DEPDC5. Through the degradation of DEPDC5, releases the GATOR1 complex-mediated inhibition of the TORC1 pathway. It is therefore an amino acid-dependent activator within the amino acid-sensing branch of the TORC1 pathway, indirectly regulating different cellular processes including cell growth and autophagy (PubMed : 29769719).
See full target information Kelch-like protein 22

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