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Rabbit Anti-Membrin antibody
Rabbit Anti-Membrin antibody
2310032N09Rik; 27 kDa Golgi SNARE protein; Bos1; EPM6; Golgi SNAP receptor complex member 2; Golgi SNARE; Gosr2; GOSR2_HUMAN; Gs27; Membrin; SNARE.
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  • NO.:SL18786R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:(predicted: Human,Mouse,Rat,Pig,Cow,Horse,Rabbit,)
    Applications:ELISA IHC-P IHC-F ICC IF
    concentration:1mg/ml
  • Goods click count:18
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Product Name Membrin
Chinese Name Membrin蛋白抗体
Alias 2310032N09Rik; 27 kDa Golgi SNARE protein; Bos1; EPM6; Golgi SNAP receptor complex member 2; Golgi SNARE; Gosr2; GOSR2_HUMAN; Gs27; Membrin; SNARE.  
Research Area Cell biology  Signal transduction  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, Mouse, Rat, Pig, Cow, Horse, Rabbit, )
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 25kDa
Cellular localization cytoplasmic 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human Membrin: 101-200/212 
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 This gene encodes a trafficking membrane protein which transports proteins among the medial- and trans-Golgi compartments. Due to its chromosomal location and trafficking function, this gene may be involved in familial essential hypertension. Three transcript variants encoding three different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

Function:
Involved in transport of proteins from the cis/medial-Golgi to the trans-Golgi network.

Subcellular Location:
Golgi apparatus membrane.

DISEASE:
Epilepsy, progressive myoclonic 6 (EPM6) [MIM:614018]: A neurologic disorder characterized by onset of ataxia in the first years of life, followed by action myoclonus and seizures later in childhood, and loss of independent ambulation in the second decade. Cognition is not usually affected, although mild memory difficulties may occur in the third decade.

Similarity:
Belongs to the GOSR2 family.

SWISS:
O14653

Gene ID:
9570

Database links:

Entrez Gene: 9570 Human

Entrez Gene: 419973 Chicken

Entrez Gene: 506198 Cow

Entrez Gene: 610436 Dog

Entrez Gene: 56494 Mouse

Entrez Gene: 64154 Rat

Omim: 604027 Human

SwissProt: O14653 Human

SwissProt: O35166 Mouse

SwissProt: O35165 Rat

Unigene: 463278 Human

Unigene: 195451 Mouse

Unigene: 13518 Rat



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