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Rabbit Anti-TM9SF4 antibody
Rabbit Anti-TM9SF4 antibody
TM9S4_HUMAN; Tm9sf4; Transmembrane 9 superfamily member 4; Transmembrane 9 superfamily protein member 4.
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  • NO.:SL8332R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Mouse,(predicted: Human,Rat,Dog,Pig,Cow,Horse,Rabbit,Sheep,)
    Applications:WB ELISA IHC-P IHC-F IF
    concentration:1mg/ml
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Details

Product Name TM9SF4
Chinese Name Transmembrane protein9家族成员4抗体
Alias TM9S4_HUMAN; Tm9sf4; Transmembrane 9 superfamily member 4; Transmembrane 9 superfamily protein member 4.  
Research Area Cell biology  immunology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Mouse,  (predicted: Human, Rat, Dog, Pig, Cow, Horse, Rabbit, Sheep, )
Applications WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:50-200 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 72kDa
Cellular localization The cell membrane 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human TM9SF4: 101-200/642 
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 Representing about 2% of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis which are thought important for seminal production and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20.

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

Similarity:
Belongs to the nonaspanin (TM9SF) family.

SWISS:
Q92544

Gene ID:
9777

Database links:

Entrez Gene: 9777 Human

Entrez Gene: 99237 Mouse

Entrez Gene: 296279 Rat

SwissProt: Q92544 Human

SwissProt: Q8BH24 Mouse

SwissProt: Q4KLL4 Rat

Unigene: 654665 Human

Unigene: 330674 Mouse

Unigene: 228942 Rat



Product Picture
Sample:
Stomach (Mouse) Lysate at 40 ug
Primary: Anti- TM9SF4 (SL8332R) at 1/1000 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 72 kD
Observed band size: 72 kD

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