Mouse/Rat IGF1 ELISA Kit

Key features and details

  • Specification: 96 Test
  • Sensitivity: 0.10 pg/ml (50 μl);0.37 pg/ml (10 μl);
  • Standard Curve Range: 21.23~300 ng/ml
  • Standard Curve Gradient: 7 Points
  • Number of Incubations: 2
  • Sample Volume: 50 μl/10 μl
  • Assay type: Sandwich Elisa
  • Operation Duration: 60min
  • Brand:
CAT.NO. : AEMY0024
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Size:
96T
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Product Details
Background

IGF-I receptor is a disulfide-linked heterotetrameric transmembrane protein consisting of two alpha and two beta subunits. Both the alpha and beta subunits are encoded within a single receptor precursor cDNA. The proreceptor polypeptide is proteolytically cleaved and disulfide-linked to yield the mature heterotetrameric receptor. The alpha subunit of IGF-I receptor is extracellular while the beta subunit has an extracellular domain, a transmembrane domain and a cytoplasmic tyrosine kinase domain. The IGF-I receptor is highly expressed in all cell types and tissues.

IGF-II R is a type I transmembrane glycoprotein that contains a 2,264 amino acid (aa) extracellular region, a 23 aa transmembrane segment segment and a 124 aa cytoplasmic tail. IGF-II R regulates many diverse biological functions that range from intracellular trafficking to the internalization of extracellular factors and modulation of cellular responses. It delivers newly synthesized M6P-tagged lysosomal enzymes from the trans-golgi network to endosomes, and facilitates the clearance of extracellular lysosomal and matrix degrading enzymes by internalization into clathrin-coated vesicles and delivery into endosomes. With respect to IGF-II biology, It would appear that IGF-II R is principally a regulator of local IGF-II levels, targeting IGF-II for destruction in lysosomes.
The heterotetrameric receptors for insulin (INS R) and IGF-I (IGF-I R) are receptor tyrosine kinases that consist of two ligandbinding alpha subunits and two beta subunits. Ligand binding induces autophosphorylation on multiple tyrosine residues of beta subunits. Phosphorylation of Tyr1162 and 1163 on INS R and Tyr1135 and 1136 on IGF-I R stimulates intrinsic kinase activity.

Typical data

ng/ml

O.D.

Average

Corrected

0.00

0.0054

0.0060

0.0057

1.23

0.0110

0.0105

0.0108

0.0051

3.07

0.0193

0.0197

0.0195

0.0138

7.68

0.0436

0.0484

0.0460

0.0403

19.20

0.1256

0.1296

0.1276

0.1219

48.00

0.4230

0.4038

0.4134

0.4077

120.00

1.3870

1.3390

1.3630

1.3573

300.00

3.3950

3.3240

3.3595

3.3538

Precision

Intra-assay Precision

Inter-assay Precision

Sample Number

S1

S2

S3

S1

S2

S3

22

22

22

6

6

6

Average(ng/ml)

6.4

28.9

120.6

6.7

30.4

127.4

Standard Deviation

0.2

1.1

5.9

0.3

1.3

5.5

Coefficient of Variation(%)

3.7

3.7

4.9

3.8

4.2

4.3

Intra-assay Precision (Precision within an assay) Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision. Inter-assay Precision (Precision between assays) Three samples of known concentration were tested six times on one plate to assess intra-assay precision.
Spike Recovery
The spike recovery was evaluated by spiking 3 levels of mouse/rat IGF-I/IGF-1 into health mouse/rat serum sample. The un-spiked serum was used as blank in this experiment.
The recovery ranged from 81% to 119% with an overall mean recovery of 99%.
Sample Values
Sample Matrix Sample Evaluated Range (ng/ml) Detectable (%) Mean of Detectable (ng/ml)
Serum 30 64.64-353.03 100 179.59

Serum/Plasma – Thirty samples from apparently healthy mice were evaluated for the presence of IGF-I/IGF-1 in this assay. No medical histories were available for the donors.

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