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Rabbit Anti-MXRA8/AF594 Conjugated antibody
Rabbit Anti-MXRA8/AF594 Conjugated antibody
FLJ41492; FLJ41492; FLJ46603; HBV PreS1 transactivated protein 1; Matrix remodelling associated 7; Matrix-remodeling-associated protein 7; MXRA7; MXRA7_HUMAN; PS1TP1; TMAP1; Transmembrane anchor protein 1.
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  • NO.:SL19118R-AF594
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Human,Mouse,(predicted: Rat,Dog,Pig,Cow,Sheep,)
    Applications:ICC IF
    concentration:1mg/ml
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Details

Product Name Anti-MXRA8/AF594
Chinese Name AF594标记的基质重塑相关蛋白8抗体
Alias FLJ41492; FLJ41492; FLJ46603; HBV PreS1 transactivated protein 1; Matrix remodelling associated 7; Matrix-remodeling-associated protein 7; MXRA7; MXRA7_HUMAN; PS1TP1; TMAP1; Transmembrane anchor protein 1.  
Research Area Cell biology  immunology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Human, Mouse,  (predicted: Rat, Dog, Pig, Cow, Sheep, )
Applications ICC=1:50-200 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Molecular weight 47kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human MXRA8
Lsotype IgG
Purification affinity purified by Protein A
Storage Buffer 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
Product Detail background:
MXRA8 is a 442 amino acid single-pass type I membrane protein that is implicated in the maintenance and maturation of the blood-brain barrier. Containing two Ig-like V-type (immunoglobulin-like) domains, MXRA8 exists as two alternatively spliced isoforms that are encoded by a gene that maps to human chromosome 1p36.33. Human chromosome 1 spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma

Function:
May play a role in the maturation and maintenance of blood-brain barrier.

Subcellular Location:
Membrane.

Similarity:
Contains 2 Ig-like V-type (immunoglobulin-like) domains.

Database links:

Entrez Gene: 54587 Human

Entrez Gene: 313770 Rat

SwissProt: Q9BRK3 Human

SwissProt: Q5XI43 Rat

Unigene: 515687 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

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