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Mouse Connexin 40 / GJA5 ELISA Kit

SKU:
MOFI00757
Product Type:
ELISA Kit
Size:
96 Assays
Uniprot:
Q01231
Sensitivity:
11.719pg/ml
Range:
19.531-1250pg/ml
ELISA Type:
Sandwich
Synonyms:
CX40, ATFB11, GJA5, alpha 5, 40kD, connexin 40, connexin-40, Connexin-40, Cx40, gap junction alpha-5 protein, gap junction protein, alpha 5, 40kDa, gap junction protein, alpha 5, 40kDa, connexin 40, MGC11185
Reactivity:
Mouse
€649
Frequently bought together:

Description

system_update_altDatasheetsystem_update_altMSDS

Mouse Connexin 40/GJA5 ELISA Kit

The Mouse Connexin-40 (GJA5) ELISA Kit is a vital tool for researchers studying connexin-40 levels in mouse serum, plasma, and cell culture supernatants. This kit offers exceptional sensitivity and specificity, ensuring accurate and reproducible results for a variety of research applications.Connexin-40 is a key protein involved in intercellular communication within the cardiovascular system, playing a crucial role in coordinating heart rhythm and blood flow.

Dysfunction of connexin-40 has been linked to various cardiovascular diseases, making it a valuable biomarker for understanding these conditions and exploring potential treatments.Overall, the Mouse Connexin-40 (GJA5) ELISA Kit is a valuable asset for researchers interested in studying the role of connexin-40 in cardiovascular health and disease.

Product Name:Mouse Connexin 40 / GJA5 ELISA Kit
Product Code:MOFI00757
Size:96 Assays
Alias:CX40, ATFB11, GJA5, alpha 5, 40kD, connexin 40, connexin-40, Connexin-40, Cx40, gap junction alpha-5 protein, gap junction protein, alpha 5, 40kDa, gap junction protein, alpha 5, 40kDa, connexin 40, MGC11185
Detection Method:Sandwich ELISA
Application:This immunoassay kit allows for the in vitro quantitative determination of Mouse CX40 concentrations in serum plasma and other biological fluids.
Sensitivity:11.719pg/ml
Range:19.531-1250pg/ml
Storage:4°C for 6 months
Note:For Research Use Only
Recovery: Matrices listed below were spiked with certain level of Mouse CX40 and the recovery rates were calculated by comparing the measured value to the expected amount of Mouse CX40 in samples.
MatrixRecovery range(%)Average(%)
serum(n=5)92-105100
EDTA plasma(n=5)96-10399
UFH plasma(n=5)87-10293
Linearity:The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Mouse CX40 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Sample1:21:41:8
serum(n=5)86-101%85-102%85-103%
EDTA plasma(n=5)86-95%83-98%82-93%
UFH plasma(n=5)81-98%80-100%80-99%
Intra Assay:CV <8%
Inter Assay:CV <10%
ComponentQuantityStorage
ELISA Microplate (Dismountable)8-12 strips4°C for 6 months
Lyophilized Standard24°C/-20°C
Sample/Standard Dilution Buffer20ml4°C
Biotin-labeled Antibody(Concentrated)120ul4°C (Protect from light)
Antibody Dilution Buffer10ml4°C
HRP-Streptavidin Conjugate(SABC)120ul4°C (Protect from light)
SABC Dilution Buffer10ml4°C
TMB Substrate10ml4°C (Protect from light)
Stop Solution10ml4°C
Wash Buffer(25X)30ml4°C
Plate Sealer5-

Other materials and equipment required:

  • Microplate reader with 450 nm wavelength filter
  • Multichannel Pipette, Pipette, microcentrifuge tubes and disposable pipette tips
  • Incubator
  • Deionized or distilled water
  • Absorbent paper
  • Buffer resevoir
UniprotQ01231
UniProt Protein Function:GJA5: One gap junction consists of a cluster of closely packed pairs of transmembrane channels, the connexons, through which materials of low MW diffuse from one cell to a neighboring cell. Defects in GJA5 are a cause of familial atrial standstill (FAS). Atrial standstill is an extremely rare arrhythmia, characterized by the absence of electrical and mechanical activity in the atria. Electrocardiographically, it is characterized by bradycardia, the absence of P waves, and a junctional narrow complex escape rhythm. Defects in GJA5 are the cause of familial atrial fibrillation type 11 (ATFB11). ATFB11 is a familial form of atrial fibrillation, a common sustained cardiac rhythm disturbance. Atrial fibrillation is characterized by disorganized atrial electrical activity and ineffective atrial contraction promoting blood stasis in the atria and reduces ventricular filling. It can result in palpitations, syncope, thromboembolic stroke, and congestive heart failure. Belongs to the connexin family. Alpha-type (group II) subfamily.
UniProt Protein Details:

Protein type:Membrane protein, integral; Motility/polarity/chemotaxis; Membrane protein, multi-pass; Channel, misc.

Cellular Component: connexon complex; cell projection; membrane; integral to plasma membrane; integral to membrane; gap junction; plasma membrane; cell junction

Molecular Function:gap junction hemi-channel activity; gap junction channel activity

Biological Process: blood vessel development; negative regulation of glomerular filtration; gap junction assembly; regulation of vasodilation; positive regulation of vasodilation; protein oligomerization; regulation of systemic arterial blood pressure; positive regulation of vasoconstriction; artery morphogenesis; regulation of systemic arterial blood pressure by renal system process; embryonic heart tube development; cell communication; negative regulation of blood pressure; skeletal development; potassium ion transport; embryonic limb morphogenesis

UniProt Code:Q01231
NCBI GenInfo Identifier:50514
NCBI Gene ID:14613
NCBI Accession:CAA43850.1
UniProt Related Accession:Q01231
Molecular Weight:40,413 Da
NCBI Full Name:Cx40
NCBI Synonym Full Names:gap junction protein, alpha 5
NCBI Official Symbol:Gja5  
NCBI Official Synonym Symbols:Cx40; Cnx40; Gja-5; 5730555N10Rik  
NCBI Protein Information:gap junction alpha-5 protein; connexin-40; gap junction membrane channel protein alpha 5
UniProt Protein Name:Gap junction alpha-5 protein
UniProt Synonym Protein Names:Connexin-40
UniProt Gene Name:Gja5  
UniProt Entry Name:CXA5_MOUSE

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

StepProcedure
1. Set standard, test sample and control (zero) wells on the pre-coated plate respectively, and then, record their positions. It is recommended to measure each standard and sample in duplicate. Wash plate 2 times before adding standard, sample and control (zero) wells!
2.Aliquot 0.1ml standard solutions into the standard wells.
3. Add 0.1 ml of Sample / Standard dilution buffer into the control (zero) well.
4. Add 0.1 ml of properly diluted sample (Human serum, plasma, tissue homogenates and other biological fluids.) into test sample wells.
5.Seal the plate with a cover and incubate at 37 °C for 90 min.
6. Remove the cover and discard the plate content, clap the plate on the absorbent filter papers or other absorbent material. Do NOT let the wells completely dry at any time. Wash plate X2.
7. Add 0.1 ml of Biotin- detection antibody working solution into the above wells (standard, test sample & zero wells). Add the solution at the bottom of each well without touching the side wall.
8.Seal the plate with a cover and incubate at 37°C for 60 min.
9. Remove the cover, and wash plate 3 times with Wash buffer. Let wash buffer rest in wells for 1 min between each wash.
10. Add 0.1 ml of SABC working solution into each well, cover the plate and incubate at 37°C for 30 min.
11. Remove the cover and wash plate 5 times with Wash buffer, and each time let the wash buffer stay in the wells for 1-2 min.
12. Add 90 µL of TMB substrate into each well, cover the plate and incubate at 37°C in dark within 10-20 min. (Note: This incubation time is for reference use only, the optimal time should be determined by end user.) And the shades of blue can be seen in the first 3-4 wells (with most concentrated standard solutions), the other wells show no obvious color.
13. Add 50 µL of Stop solution into each well and mix thoroughly. The color changes into yellow immediately.
14. Read the O.D. absorbance at 450 nm in a microplate reader immediately after adding the stop solution.

When carrying out an ELISA assay it is important to prepare your samples in order to achieve the best possible results. Below we have a list of procedures for the preparation of samples for different sample types.

Sample Type Protocol
Serum:

If using serum separator tubes, allow samples to clot for 30 minutes at room temperature. Centrifuge for 10 minutes at 1,000x g. Collect the serum fraction and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles.

If serum separator tubes are not being used, allow samples to clot overnight at 2-8°C. Centrifuge for 10 minutes at 1,000x g. Remove serum and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles.

Plasma:

Collect plasma using EDTA or heparin as an anticoagulant. Centrifuge samples at 4°C for 15 mins at 1000 - g within 30 mins of collection. Collect the plasma fraction and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles. Note: Over haemolysed samples are not suitable for use with this kit.

Urine & Cerebrospinal Fluid:

Collect the urine (mid-stream) in a sterile container, centrifuge for 20 mins at 2000-3000 rpm. Remove supernatant and assay immediately. If any precipitation is detected, repeat the centrifugation step. A similar protocol can be used for cerebrospinal fluid.

Cell culture supernatant:

Collect the cell culture media by pipette, followed by centrifugation at 4°C for 20 mins at 1500 rpm. Collect the clear supernatant and assay immediately.

Cell lysates:

Solubilize cells in lysis buffer and allow to sit on ice for 30 minutes. Centrifuge tubes at 14,000 x g for 5 minutes to remove insoluble material. Aliquot the supernatant into a new tube and discard the remaining whole cell extract. Quantify total protein concentration using a total protein assay. Assay immediately or aliquot and store at ≤ -20°C.

Tissue homogenates:

The preparation of tissue homogenates will vary depending upon tissue type. Rinse tissue with 1X PBS to remove excess blood & homogenize in 20ml of 1X PBS (including protease inhibitors) and store overnight at ≤ -20°C. Two freeze-thaw cycles are required to break the cell membranes. To further disrupt the cell membranes you can sonicate the samples. Centrifuge homogenates for 5 mins at 5000xg. Remove the supernatant and assay immediately or aliquot and store at -20°C or -80°C.

Tissue lysates:

Rinse tissue with PBS, cut into 1-2 mm pieces, and homogenize with a tissue homogenizer in PBS. Add an equal volume of RIPA buffer containing protease inhibitors and lyse tissues at room temperature for 30 minutes with gentle agitation. Centrifuge to remove debris. Quantify total protein concentration using a total protein assay. Assay immediately or aliquot and store at ≤ -20 °C.

Breast Milk:

Collect milk samples and centrifuge at 10,000 x g for 60 min at 4°C. Aliquot the supernatant and assay. For long term use, store samples at -80°C. Minimize freeze/thaw cycles.

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