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hnRNP K Colorimetric Cell-Based ELISA Kit

SKU:
CBCAB00696
Product Type:
ELISA Kit
ELISA Type:
Cell Based
Research Area:
Immunology
Reactivity:
Human
Mouse
Rat
Detection Method:
Colorimetric
$719
Frequently bought together:

Description

system_update_altDatasheetMSDS

hnRNP K Colorimetric Cell-Based ELISA Kit

The HNRNP-K Colorimetric Cell-based ELISA Kit offered by Assay Genie is a reliable and accurate tool for detecting HNRNP-K levels in cell samples. HNRNP-K, also known as heterogeneous nuclear ribonucleoprotein K, is a key protein involved in RNA processing and gene expression regulation.This easy-to-use kit provides high sensitivity and specificity, allowing for precise measurements of HNRNP-K levels in cell lysates.

With its user-friendly protocol and fast results, this kit is ideal for researchers studying RNA metabolism, gene regulation, and RNA-binding proteins.Gain valuable insights into the role of HNRNP-K in cellular processes and disease pathogenesis with the HNRNP-K Colorimetric Cell-based ELISA Kit from Assay Genie. Be confident in your results and accelerate your research with this innovative tool.

Product Name:hnRNP K Colorimetric Cell-Based ELISA
Product Code:CBCAB00696
ELISA Type:Cell-Based
Target:hnRNP K
Reactivity:Human, Mouse, Rat
Dynamic Range:> 5000 Cells
Detection Method:Colorimetric 450 nmStorage/Stability:4°C/6 Months
Format:96-Well Microplate

The hnRNP K Colorimetric Cell-Based ELISA Kit is a convenient, lysate-free, high throughput and sensitive assay kit that can detect hnRNP K protein expression profile in cells. The kit can be used for measuring the relative amounts of hnRNP K in cultured cells as well as screening for the effects that various treatments, inhibitors (ie siRNA or chemicals), or activators have on hnRNP K.

Qualitative determination of hnRNP K concentration is achieved by an indirect ELISA format. In essence, hnRNP K is captured by hnRNP K-specific primary antibodies while the HRP-conjugated secondary antibodies bind the Fc region of the primary antibody. Through this binding, the HRP enzyme conjugated to the secondary antibody can catalyze a colorimetric reaction upon substrate addition. Due to the qualitative nature of the Cell-Based ELISA, multiple normalization methods are needed:

1. A monoclonal antibody specific for human GAPDH is included to serve as an internal positive control in normalizing the target absorbance values.
2. Following the colorimetric measurement of HRP activity via substrate addition, the Crystal Violet whole-cell staining method may be used to determine cell density. After staining, the results can be analysed by normalizing the absorbance values to cell amounts, by which the plating difference can be adjusted.
Database Information:Gene ID: 3190, UniProt ID: P61978, OMIM: 600712, Unigene: Hs.522257
Gene Symbol:HNRNPK
Sub Type:None
UniProt Protein Function:hnRNP K: a heterogeneous nuclear ribonucleoprotein (hnRNP). One of the major pre-mRNA-binding proteins. Binds tenaciously to poly(C) sequences. Likely to play a role in the nuclear metabolism of hnRNAs, particularly for pre-mRNAs that contain cytidine-rich sequences. Can also bind poly(C) single-stranded DNA. Two alternatively spliced isoforms have been described.
UniProt Protein Details:

Protein type:RNA splicing; RNA-binding; Spliceosome

Chromosomal Location of Human Ortholog: 9q21.32

Cellular Component: cell-cell adherens junction; extracellular matrix; focal adhesion; membrane; nuclear chromatin; nucleoplasm; nucleus

Molecular Function:protein binding; RNA binding; single-stranded DNA binding

Biological Process: gene expression; negative regulation of apoptosis; nuclear mRNA splicing, via spliceosome; positive regulation of low-density lipoprotein receptor biosynthetic process; positive regulation of receptor-mediated endocytosis; positive regulation of transcription from RNA polymerase II promoter; protein sumoylation; RNA processing; signal transduction

Disease: Au-kline Syndrome

NCBI Summary:This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene is located in the nucleoplasm and has three repeats of KH domains that binds to RNAs. It is distinct among other hnRNP proteins in its binding preference; it binds tenaciously to poly(C). This protein is also thought to have a role during cell cycle progession. Several alternatively spliced transcript variants have been described for this gene, however, not all of them are fully characterized. [provided by RefSeq, Jul 2008]
UniProt Code:P61978
NCBI GenInfo Identifier:48429103
NCBI Gene ID:3190
NCBI Accession:P61978.1
UniProt Secondary Accession:P61978,Q07244, Q15671, Q59F98, Q5T6W4, Q60577, Q922Y7 Q96J62,
UniProt Related Accession:P61978
Molecular Weight:48,562 Da
NCBI Full Name:Heterogeneous nuclear ribonucleoprotein K
NCBI Synonym Full Names:heterogeneous nuclear ribonucleoprotein K
NCBI Official Symbol:HNRNPK  
NCBI Official Synonym Symbols:AUKS; CSBP; TUNP; HNRPK  
NCBI Protein Information:heterogeneous nuclear ribonucleoprotein K
UniProt Protein Name:Heterogeneous nuclear ribonucleoprotein K
UniProt Synonym Protein Names:Transformation up-regulated nuclear protein; TUNP
Protein Family:Heterogeneous nuclear ribonucleoprotein
UniProt Gene Name:HNRNPK  
ComponentQuantity
96-Well Cell Culture Clear-Bottom Microplate2 plates
10X TBS24 mL
Quenching Buffer24 mL
Blocking Buffer50 mL
15X Wash Buffer50 mL
Primary Antibody Diluent12 mL
100x Anti-Phospho Target Antibody 60 µL
100x Anti-Target Antibody60 µL
Anti-GAPDH Antibody60 µL
HRP-Conjugated Anti-Rabbit IgG Antibody12 mL
HRP-Conjugated Anti-Mouse IgG Antibody12 mL
SDS Solution12 mL
Stop Solution24 mL
Ready-to-Use Substrate12 mL
Crystal Violet Solution12 mL
Adhesive Plate Seals2 seals

The following materials and/or equipment are NOT provided in this kit but are necessary to successfully conduct the experiment:

  • Microplate reader able to measure absorbance at 450 nm and/or 595 nm for Crystal Violet Cell Staining (Optional)
  • Micropipettes with capability of measuring volumes ranging from 1 µL to 1 ml
  • 37% formaldehyde (Sigma Cat# F-8775) or formaldehyde from other sources
  • Squirt bottle, manifold dispenser, multichannel pipette reservoir or automated microplate washer
  • Graph paper or computer software capable of generating or displaying logarithmic functions
  • Absorbent papers or vacuum aspirator
  • Test tubes or microfuge tubes capable of storing ≥1 ml
  • Poly-L-Lysine (Sigma Cat# P4832 for suspension cells)
  • Orbital shaker (optional)
  • Deionized or sterile water

*Note: Protocols are specific to each batch/lot. For the correct instructions please follow the protocol included in your kit.

StepProcedure
1.Seed 200 µL of 20,000 adherent cells in culture medium in each well of a 96-well plate. The plates included in the kit are sterile and treated for cell culture. For suspension cells and loosely attached cells, coat the plates with 100 µL of 10 µg/ml Poly-L-Lysine (not included) to each well of a 96-well plate for 30 minutes at 37°C prior to adding cells.
2.Incubate the cells for overnight at 37°C, 5% CO2.
3.Treat the cells as desired.
4.Remove the cell culture medium and rinse with 200 µL of 1x TBS, twice.
5.Fix the cells by incubating with 100 µL of Fixing Solution for 20 minutes at room temperature. The 4% formaldehyde is used for adherent cells and 8% formaldehyde is used for suspension cells and loosely attached cells.
6.Remove the Fixing Solution and wash the plate 3 times with 200 µL 1x Wash Buffer for five minutes each time with gentle shaking on the orbital shaker. The plate can be stored at 4°C for a week.
7.Add 100 µL of Quenching Buffer and incubate for 20 minutes at room temperature.
8.Wash the plate 3 times with 1x Wash Buffer for 5 minutes each time.
9.Add 200 µL of Blocking Buffer and incubate for 1 hour at room temperature.
10. Wash 3 times with 200 µL of 1x Wash Buffer for 5 minutes each time.
11.Add 50 µL of 1x primary antibodies (Anti-hnRNP K Antibody and/or Anti-GAPDH Antibody) to the corresponding wells, cover with Parafilm and incubate for 16 hours (overnight) at 4°C. If the target expression is known to be high, incubate for 2 hours at room temperature.
12.Wash 3 times with 200 µL of 1x Wash Buffer for 5 minutes each time.
13.Add 50 µL of 1x secondary antibodies (HRP-Conjugated AntiRabbit IgG Antibody or HRP-Conjugated Anti-Mouse IgG Antibody) to corresponding wells and incubate for 1.5 hours at room temperature.
14.Wash 3 times with 200 µL of 1x Wash Buffer for 5 minutes each time.
15.Add 50 µL of Ready-to-Use Substrate to each well and incubate for 30 minutes at room temperature in the dark.
16.Add 50 µL of Stop Solution to each well and read OD at 450 nm immediately using the microplate reader.

(Additional Crystal Violet staining may be performed if desired – details of this may be found in the kit technical manual.)

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