Monkey Polymorphonuclear Elastase ELISA Kit | PMN elisa kit

Monkey Polymorphonuclear Elastase ELISA Kit

Cat. Num. AAA44341

• Gene Names: Tbce; pmn; 2610206D02Rik; C530005D02Rik
• Reactivity: Monkey
• Synonyms: Polymorphonuclear Elastase; Monkey Polymorphonuclear Elastase ELISA Kit; PMN elisa kit

• Reactivity: Monkey
• Sequence Length: 270

• Assay Type: Quantitative Sandwich
• Detection Range: 6.25ng/ml-200ng/ml
• Sensitivity: 1.0ng/ml
• Intra-assay Precision: Intra-assay CV (%) is less than 15%.
• Inter-assay Precision: Inter-assay CV (%) is less than 15%. [CV(%) = SD/mean ×100]. All CV% should be compared by concentration, not compared by OD values.
• Preparation and Storage: Store all reagents at 2-8 degree C

Typical Testing Data/Standard Curve (for reference only)

Related Product Information for PMN elisa kit

Background/Introduction: This Quantitative Sandwich ELISA kit is for lab reagent/research use only, not for drug, household, therapeutic or test applications! This kit is intended to be used for determine the level of PMN (hereafter termed "analyte") in undiluted original Monkey serum, plasma or tissue homogenates samples. For other sample types please contact tech support to determine compatibility with this assay. This kit is not suitable for assaying non-biological sources of substances.

NCBI and Uniprot Product Information

• NCBI GI #: 568982038
• NCBI GeneID: 70430
• NCBI Accession #: XP_006516838.1
• NCBI GenBank Nucleotide #: XM_006516775.1
• UniProt Accession #: Q8CIV8
• Molecular Weight: 59,086 Da
• NCBI Official Full Name: tubulin-specific chaperone E isoform X3
• NCBI Official Synonym Full Names: tubulin-specific chaperone E
• NCBI Official Symbol: Tbce
• NCBI Official Synonym Symbols: pmn; 2610206D02Rik; C530005D02Rik
• NCBI Protein Information: tubulin-specific chaperone E; tubulin-folding cofactor E; progressive motor neuropathy
• UniProt Protein Name: Tubulin-specific chaperone E
• UniProt Gene Name: Tbce
• UniProt Entry Name: TBCE_MOUSE

NCBI Description

This gene encodes a tubulin binding cofactor that participates in microtubule dynamics. A mouse model of progressive motor neuropathy (pmn) was discovered to harbor a single amino acid deletion in this gene. Mice that are homozygous for pmn allele exhibit progressive atrophy and premature death due to respiratory failure. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2015]

Uniprot Description

TBCE: Tubulin-folding protein; involved in the second step of the tubulin folding pathway. Seems to be implicated in the maintenance of the neuronal microtubule network. Involved in regulation of tubulin heterodimer dissociation. Defects in TBCE are a cause of hypoparathyroidism- retardation-dysmorphism syndrome (HRD); also known as hypoparathyroidism with short stature, mental retardation, and seizures or Sanjad-Sakati syndrome. HRD is an autosomal recessive disorder reported almost exclusively in Middle Eastern populations. Defects in TBCE are the cause of Kenny-Caffey syndrome type 1 (KCS1). KCS1 is similar to HRD with the additional features of osteosclerosis and recurrent bacterial infections. Belongs to the TBCE family.

Protein type: Chaperone

Cellular Component: cytoskeleton; cytoplasm

Molecular Function: unfolded protein binding

Biological Process: tubulin folding; developmental growth; protein folding; axonogenesis; adult locomotory behavior; muscle atrophy; microtubule cytoskeleton organization and biogenesis; peripheral nervous system neuron axonogenesis; post-chaperonin tubulin folding pathway; post-embryonic development