IGF2 rabbit pAb

CAT: 0855-ES10707-01Size: 50 µLDry Ice: NoHazardous: No
CAT#:0855-ES10707-01Size:50 µL
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Background
This gene encodes a member of the insulin family of polypeptide growth factors, which are involved in development and growth. It is an imprinted gene, expressed only from the paternal allele, and epigenetic changes at this locus are associated with Wilms tumour, Beckwith-Wiedemann syndrome, rhabdomyosarcoma, and Silver-Russell syndrome. A read-through INS-IGF2 gene exists, whose 5' region overlaps the INS gene and the 3' region overlaps this gene. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2010]
Description
This gene encodes a member of the insulin family of polypeptide growth factors, which are involved in development and growth. It is an imprinted gene, expressed only from the paternal allele, and epigenetic changes at this locus are associated with Wilms tumour, Beckwith-Wiedemann syndrome, rhabdomyosarcoma, and Silver-Russell syndrome. A read-through INS-IGF2 gene exists, whose 5' region overlaps the INS gene and the 3' region overlaps this gene. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2010],
UniProt
P01344
Swiss Prot
P01344
Reactivity
Human; Mouse; Rat; Pig
Immunogen
Synthesized peptide derived from part region of human protein AA range: 25-40
Target
IGF-2
Clonality
Polyclonal
Source
Rabbit
Applications
WB; ELISA
Concentration
1 mg/ml
Dilution
WB 1:500-2000 ELISA 1:5000-20000
Buffer
-20°C/1 year
Molecular Weight
10 or 19 Kd
Storage Conditions
-20°C/1 year
Observed Molecular Weight
10 or 19 Kd
Fragment
IgG
Subcellular Location
Secreted .
Gene ID (Human)
3481

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