Anti-FSD2 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

BOSSBS-13222R-A750

Anti-FSD2 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

BOSSBS-13222R-A750

Antibody type:
Primary
Antigen name:
FSD2
Clonality:
Polyclonal
Conjugation:
Alexa Fluor® 750
Host:
Rabbit
ImmunoChemistry:
Yes
ImmunoFluorescence:
Yes
Isotype:
IgG
Reactivity:
Western blot:
Yes
Environmentally Preferable:
Epitope:
221-320/749
Form:
Liquid
Gene ID:
123722
Antigen synonyms:
RP11-127F21|Fibronectin type III and SPRY domain containing protein 2|SPRY domain containing 1|Fibronectin type III and SPRY domain containing 2|SPRY domain containing protein 1|SPRYD1
Modification:
Unmodified
Storage buffer:
Aqueous buffered solution containing 0,01M TBS (pH 7,4) with 1% BSA, 0,03% Proclin300 and 50% Glycerol.
Molecular weight:
85 kDa
Storage temperature:
Store at −20 °C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
Concentration:
1 µg/µl
Shipping temperature:
4 °C
Immunogen:
KLH conjugated synthetic peptide derived from human FSD2
Tested applications:
ICC
Purification:
Purified by Protein A
Pack type:
Vial
Pk:
100 µl

FSD2 is a 749 amino acid protein containing one B30.2/SPRY domain and two fibronectin type-III domains. The gene encoding FSD2 maps to human chromosome 15q25.2. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and consists of about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are also associated with chromosome 15.

Type: Primary
Antigen: FSD2
Clonality: Polyclonal
Clone:
Conjugation: ALEXA FLUOR® 750
Public Immunogen Range: 221-320/749
Host: Rabbit
Isotype: IgG
Reactivity: