SAMD9 Polyclonal Antibody, HRP Conjugated
Product Specifications
Background
Defects in SAMD9 are the cause of normophosphatemic familial tumoral calcinosis (NFTC) . NFTC is an uncommon life-threatening disorder characterized by massive periarticular, and seldom visceral, deposition of calcified tumors.
Synonyms
SAM domain-containing protein 9; SAMD9; SAMD9_HUMAN; sterile alpha mot domain containing 9; Sterile alpha mot domain-containing protein 9; C7orf5.
Gene ID
54809
Host
Rabbit
Cross Reactivity
Human, Mouse, Rat
Immunogen
1501-1589/1589
Target
SAMD9
Clonality
Polyclonal
Isotype
IgG
Conjugation
HRP
Source
KLH conjugated synthetic peptide derived from human SAMD9
Applications
ELISA, IHC-P, IHC-F
Purification
Purified by Protein A.
Concentration
1µg/µl
Dilution
ELISA (ELISA=1:5000-10000), IHC-P (IHC-P=1:100-500), IHC-F (IHC-F=1:100-500)
Buffer
Aqueous buffered solution containing 0.01M TBS (pH 7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Modification
Unmodified
Storage Conditions
Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
Gene ID URL
54809
Curated Selection
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