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Rabbit Anti-SLC44A4/AP Conjugated antibody
Rabbit Anti-SLC44A4/AP Conjugated antibody
Solute carrier family 44, member 4;SLC44A4;CTL4;FLJ14491;NG22; CTL4_HUMAN.
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  • NO.:SL13961R-AP
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:(predicted: Human,Mouse,Rat,Horse,)
    Applications:WB IHC-P IHC-F ICC
    concentration:1mg/ml
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Details

Product Name Anti-SLC44A4/AP
Chinese Name 碱性磷酸酶(AP)标记的胆碱转运体样蛋白4
Alias Solute carrier family 44, member 4; SLC44A4; CTL4; FLJ14491; NG22; CTL4_HUMAN.  
Research Area Tumour  Cell biology  lymphocyte  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, Mouse, Rat, Horse, )
Applications WB=1:50-200 IHC-P=1:50-200 IHC-F=1:50-200 ICC=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Molecular weight 79kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human SLC44A4
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:
Choline is an essential nutrient that is required for the synthesis of both acetylcholine, a neurotransmitter found in cholinergic nerve terminals, and phosphatidylcholine, a key component of cell membranes. Choline deficiencies are associated with defects in cell growth and have been implicated in disorders such as Alzheimer’s and Parkinson’s disease. The choline transporter-like protein family (CTL) are solute carriers that transport choline, a compound which is not able to permeate cells, across the cell membrane. CTL4, also known as SLC44A4 (Solute carrier family 44 member 4), is a multi-pass membrane protein which can fuse with Neu1, generating a CTL4-Neu1 transcript. This fusion is implicated in sialidosis, a disease characterized by improper lysosomal storage.

Subcellular Location:
Membrane; Multi-pass membrane protein (By similarity).

DISEASE:
Note=An interstitial deletion causing the fusion of exon 10 of CTL4 with the 3'-UTR of NEU has been detected in two patients affected by sialidosis.

Similarity:
Belongs to the CTL (choline transporter-like) family.

Database links:
 

UniProtKB/Swiss-Prot: Q53GD3.2



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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