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AN301321L

Recombinant Phospho-DRP1 (Ser616) Monoclonal Antibody

Size

£311.40

Was £346.00

SKU:
AN301321L
Additional Names:
DRP,DLP,DNM1L,DLP1,DRP1,DVLP,DYMPLE,EMPF,EMPF1,HDYNIV,Dnm1p/Vps1p-like protein (DVLP),dynamin 1 like,Dynamin family member proline-rich carboxyl-terminal domain less (Dymple),Dynamin-1-like protein,Dynamin-like protein,DLP1,DRP1,DVLP,DYMPLE,dynamin 1 like,EMPF,EMPF1,HDYNIV,Dnm1p/Vps1p-like protein,dnml1,Dynamin family member proline-rich carboxyl-terminal domain less,Dynamin like protein,Dynamin related protein 1,Dynamin-like protein 4,Dynamin-like protein IV,Dynamin-related protein 1,DYNIV
Application:
WB
Concentration:
0.2 mg/ml
Purification:
Protein A Purified
Storage Conditions:
-20[o]C Avoid freeze/thaw cycles.
Supplier:
Elabscience
Host:
Rabbit
Reactivities:
Human, Mouse, Rat
Buffer:
PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.
Immunogen:
A synthetic peptide corresponding to residues around (Ser616) of Human Phospho-DRP1
Clone:
B1084
Uniprot:
O00429
Synonyms:
DLP1;Dnm1p/Vps1p-like protein;DRP1;DVLP;DYMPLE;dynamin family member proline-rich carboxyl-terminal domain less;dynamin-1-like protein;Dynamin-like protein;dynamin-like protein 4;dynamin-like protein IV;dynamin-related protein 1;EMPF;EMPF1;HDYNIV;OPA5
Extra Details:
This gene encodes a member of the dynamin superfamily of GTPases. The encoded protein mediates mitochondrial and peroxisomal division, and is involved in developmentally regulated apoptosis and programmed necrosis. Dysfunction of this gene is implicated in several neurological disorders, including Alzheimer&apos,s disease. Mutations in this gene are associated with the autosomal dominant disorder, encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission (EMPF). Alternative splicing results in multiple transcript variants encoding different isoforms.
Shipping Conditions:
Blue Ice