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Rabbit Anti-SCFD2/AF594 Conjugated antibody
Rabbit Anti-SCFD2/AF594 Conjugated antibody
FLJ21060; FLJ39514; SCFD 2; Scfd2; SCFD2_HUMAN; Sec1 family domain containing 2; Sec1 family domain containing protein 2; Sec1 family domain-containing protein 2; STXBP1L1; Syntaxin binding protein 1 like 1; Syntaxin-binding protein 1-like 1.
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  • NO.:SL17281R-AF594
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Human,Mouse,Rat,(predicted: Dog,Pig,Cow,Horse,Sheep,)
    Applications:ICC IF
    concentration:1mg/ml
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Details

Product Name Anti-SCFD2/AF594
Chinese Name AF594标记的突触Binding protein1样1抗体
Alias FLJ21060; FLJ39514; SCFD 2; Scfd2; SCFD2_HUMAN; Sec1 family domain containing 2; Sec1 family domain containing protein 2; Sec1 family domain-containing protein 2; STXBP1L1; Syntaxin binding protein 1 like 1; Syntaxin-binding protein 1-like 1.  
Research Area Cell biology  immunology  Signal transduction  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Human, Mouse, Rat,  (predicted: Dog, Pig, Cow, Horse, 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 75kDa
Form Lyophilized or Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human SCFD2
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:
SCFD2 is a 684 amino acid protein suggested to play a role in protein transport. Existing as two alternatively spliced isoforms, SCFD2 is a member of the STXBP/unc-18/SEC1 family and is encoded by a gene that maps to human chromosome 4q12. Chromosome 4 represents approximately 6% of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.

Function:
May be involved in protein transport.

Similarity:
Belongs to the STXBP/unc-18/SEC1 family.

Database links:

Entrez Gene: 152579 Human

SwissProt: Q8WU76 Human

Unigene: 302287 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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