SAMD9 Polyklonale Antilichaam, FITC Vervoeging

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.

SAM domain-containing protein 9; SAMD9; SAMD9_HUMAN; sterile alpha mot domain containing 9; Sterile alpha mot domain-containing protein 9; C7orf5.

54809

Human, Mouse, Rat

1501-1589/1589

SAMD9

FITC

KLH conjugated synthetic peptide derived from human SAMD9

IF

Purified by Protein A.

494nm/518nm

1µg/µl

IF (IF=1:50-200)

Aqueous buffered solution containing 0.01M TBS (pH 7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

Unmodified

Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

54809