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SAMD9 Polyclonal Antibody, Cy5.5 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

Cy5.5

Source

KLH conjugated synthetic peptide derived from human SAMD9

Applications

IF

Purification

Purified by Protein A.

Excitation Emission

675nm/694nm

Concentration

1µg/µl

Dilution

IF (IF=1:50-200)

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

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