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GOT1L1 (GeneName), Putative aspartate aminotransferase, cytoplasmic 2 (ProteinName), AATC2_HUMAN.
Product Name:

Human GOT1L1/ Putative aspartate aminotransferase, cytoplasmic 2 ELISA Kit

Cat.#:

E2107h

Brand:
EIAab®
Regulatory Status:
Alternative:

Glutamate oxaloacetate transaminase 1-like protein 1, Transaminase A-like protein 1

Detection Method:
ELISA
Assay Type:
Sandwich
Detection Range:
3.9-250pg/mL
Sensitivity:
3pg/mL
Specificity:
Natural and recombinant human Putative aspartate aminotransferase, cytoplasmic 2
Sample Type:
Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Sample Data:
Assay Procedure:
Assay Procedure
Research Area:
-
Human GOT1L1 ELISA Kit
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Product Datasheets
Instruction: Down Instruction
MSDS: MSDS


Precision

Intra-assay Precision (Precision within an assay):Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision.

Intra-Assay CV: ≤3.3%

Inter-assay Precision (Precision between assays):Three samples of known concentration were tested in five separate assays to assess inter-assay precision.

Inter-Assay CV: ≤5.8%

Recovery
Recovery was determined by spiking various levels of Putative aspartate aminotransferase, cytoplasmic 2 into serum and plasma.

Sample Type

Average(%)

Recovery Range(%)

Serum

97

91-103

Plasma

99

93-105

 

 

 

 

Linearity
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Putative aspartate aminotransferase, cytoplasmic 2 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

Sample

1:2

1:4

1:8

1:16

serum(n=5)

99-109%

85-98%

104-114%

111-123%

EDTA plasma(n=5)

98-108%

104-112%

95-104%

86-97%

heparin plasma(n=5)

98-108%

 

109-118%

89-102%

87-97%

 

General Annotation


Sub Unit:
Homodimer.


Function:
N/A


Subcellular Location:
Cytoplasm


This product has not yet been referenced specifically in any publications.

[1].
"Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences."

[2].
"Architecture of the human interactome defines protein communities and disease networks."

[3].
"Biosynthesis of D-aspartate in mammals: the rat and human homologs of mouse aspartate racemase are not responsible for the biosynthesis of D-aspartate."

[4].
"Proteomic analysis identifies dysfunction in cellular transport, energy, and protein metabolism in different brain regions of atypical frontotemporal lobar degeneration."

[5].
"Targeted ubiquitination and degradation of G-protein-coupled receptor kinase 5 by the DDB1-CUL4 ubiquitin ligase complex."

[6].
"Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium."

[7].
"DNA sequence and analysis of human chromosome 8."

[8].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[9].
"Localization of the structural genes for hexokinase-1 and inorganic pyrophosphatase on region (pter-->q24) of human chromosome 10."
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