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Rabbit Anti-MCTP2 antibody
Rabbit Anti-MCTP2 antibody
FLJ11175; FLJ33303; MGC111402; Multiple C2 and transmembrane domain containing protein 2; Multiple C2 domains, transmembrane 2; Multiple C2-domains with two transmembrane regions 2.
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  • NO.:SL18738R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:(predicted: Human,Mouse,Rat,Dog,Sheep,)
    Applications:ELISA IHC-P IHC-F ICC IF
    concentration:1mg/ml
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Details

Product Name MCTP2
Chinese Name MCTP2蛋白抗体
Alias FLJ11175; FLJ33303; MGC111402; Multiple C2 and transmembrane domain containing protein 2; Multiple C2 domains, transmembrane 2; Multiple C2-domains with two transmembrane regions 2.  
Research Area Cell biology  Signal transduction  Binding protein  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, Mouse, Rat, Dog, Sheep, )
Applications ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 100kDa
Cellular localization The cell membrane 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human MCTP2: 601-700/878 
Lsotype IgG
Purification affinity purified by Protein A
Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
Product Detail MCTP2 is an 878 amino acid multi-pass membrane protein that belongs to the MCTP family. Existing as five alternatively spliced isoforms, MCTP1 binds calcium via its C2 domains in the absence of phospholipids, and is encoded by a gene that maps to human chromosome 15q26.2. Chromosome 15 houses over 700 genes and comprises nearly 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.

Function:
MCTP2 contains C2 domains which bind calcium in the absence of phospholipids. There are 5 isoforms produced by alternative splicing.

Subcellular Location:
Cell Membrane; multipass membrane protein

Similarity:
Belongs to the MCTP family.
Contains 3 C2 domains.

SWISS:
Q6DN12

Gene ID:
55784

Database links:

Entrez Gene: 55784 Human

Entrez Gene: 244049 Mouse

Entrez Gene: 308742 Rat

SwissProt: Q6DN12 Human

SwissProt: Q5RJH2 Mouse

Unigene: 592017 Human



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