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AB259152

Human SPCS1 knockout HEK-293T cell lysate

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SPCS1 KO cell lysate available now. KO validated by. Free of charge wild type control included. Knockout achieved by using CRISPR/Cas9, 1 bp insertion in exon 1 and 2 bp deletion in exon 1.

View Alternative Names

HSPC033, Microsomal signal peptidase 12 kDa subunit, OTTHUMP00000206959, SPC1, SPC12, SPCS1_HUMAN, SPase 12 kDa subunit, Signal peptidase complex subunit 1, YJR010C-A, signal peptidase 12kDa, signal peptidase complex subunit 1 homolog (S. cerevisiae)

2 Images
Sanger Sequencing - Human SPCS1 knockout HEK-293T cell lysate (AB259152)
  • Sanger seq

Unknown

Sanger Sequencing - Human SPCS1 knockout HEK-293T cell lysate (AB259152)

Allele-1 : 2 bp deletion in exon 1

Sanger Sequencing - Human SPCS1 knockout HEK-293T cell lysate (AB259152)
  • Sanger seq

Unknown

Sanger Sequencing - Human SPCS1 knockout HEK-293T cell lysate (AB259152)

Allele-2 : 1 bp insertion in exon 1

Key facts

Cell type

HEK-293T

Species or organism

Human

Tissue

Kidney

Knockout validation

Sanger Sequencing

Mutation description

Knockout achieved by using CRISPR/Cas9, 1 bp insertion in exon 1 and 2 bp deletion in exon 1.

Product details

Knockout cell lysate achieved by CRISPR/Cas9.

REACH authorisation
Abcam has not and does not intend to apply for the REACH Authorisation of customers' uses of products that contain European Authorisation list (Annex XIV) substances.
It is the responsibility of our customers to check the necessity of application of REACH Authorisation, and any other relevant authorisations, for their intended uses.

Lysate preparation: Our lysates are made using RIPA buffer to which we add a protease inhibitor cocktail and phosphatase inhibitor cocktail (ratio: 300:100:10). This means that the protein of interest is denatured. If you require a native form of the protein please use the live cell version. Please refer to our lysis protocol for further details on how our lysates are prepared.

User storage instructions: Lyophilizate may be stored at 4°C. After reconstitution, store at -20°C for short-term storage or -80°C for long-term storage.

This product is subject to limited use licenses from The Broad Institute, ERS Genomics Limited and Sigma-Aldrich Co. LLC, and is developed with patented technology. For full details of the licenses and patents please refer to our limited use license and patent pages.

What's included?

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Properties and storage information

Gene name
SPCS1
Gene editing type
Knockout
Gene editing method
CRISPR technology
Knockout validation
Sanger Sequencing
Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C

Supplementary information

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

Signal peptidase complex subunit 1 (SPCS1) also known as SPC18 is a protein with an approximate mass of 22 kDa. It forms a part of the signal peptidase complex in the endoplasmic reticulum of eukaryotic cells. This protein assists in the cleavage of signal peptides from nascent proteins being synthesized. SPCS1 is ubiquitously expressed across various tissues which indicates its significance in general cellular processes.
Biological function summary

SPCS1 supports the proper processing and maturation of secretory and membrane proteins. As a constituent of the signal peptidase complex SPCS1 participates directly in the co-translational removal of signal peptides. This functionality is integral for protein targeting and trafficking ensuring that proteins reach their intended locations within the cell or are secreted outside.

Pathways

SPCS1 is involved in the protein processing pathway within the endoplasmic reticulum. This pathway plays a role in maintaining cellular protein homeostasis. The function of SPCS1 makes it relevant to the unfolded protein response pathway indirectly influencing pathways that involve stress response and protein folding. Proteins like SEC61 which form the translocon complex work closely with SPCS1 in these pathways to facilitate protein synthesis and translocation across the ER membrane.

Disruptions in the function of SPCS1 can relate to certain neurodegenerative diseases due to its role in protein processing. Improper protein cleavage and folding could contribute to conditions such as Alzheimer's disease. Additionally the dysregulation of SPCS1 is connected to cancer where anomalies in protein maturation pathways may lead to uncontrolled cell growth. In these contexts SPCS1 abnormalities may be associated with other proteins such as tau in Alzheimer's disease and various oncogenes or tumor suppressor proteins in cancer.

Quality control

STR analysis

CSF1PO, D13S317, D7S820, D5S818, TH01, D16S539, TPOX

Cell culture

Biosafety level

EU: 2 US: 2

Adherent/suspension

Adherent

Gender

Female

Product protocols

Product promise

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For full details, please see our Terms & Conditions

Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.

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