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ELK Biotechnology
SKU:ES13355
ROM1 rabbit pAb
ROM1 rabbit pAb
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$250.00 USD
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Applications: WB
Reactivity: Human; Mouse;Rat;C. parvum
Source: Rabbit
Dilution: WB 1：500-2000
Immunogen: Synthesized peptide derived from human ROM1 AA range: 163-213
Storage_stability: -20°C/1 year
Clonality: Polyclonal
Isotype: IgG
Concentration: 1 mg/ml
Human_gene_id: 6094
Human_swiss_prot_no: Q03395
Subcellular_location: Photoreceptor inner segment membrane ; Multi-pass membrane protein . Photoreceptor outer segment membrane ; Multi-pass membrane protein .
Background: This gene is a member of a photoreceptor-specific gene family and encodes an integral membrane protein found in the photoreceptor disk rim of the eye. This protein can form homodimers or can heterodimerize with another photoreceptor, retinal degeneration slow (RDS). It is essential for disk morphogenesis, and may also function as an adhesion molecule involved in the stabilization and compaction of outer segment disks or in the maintenance of the curvature of the rim. Certain defects in this gene have been associated with the degenerative eye disease retinitis pigmentosa. [provided by RefSeq, Jul 2008],
Reactivity: Human; Mouse;Rat;C. parvum
Source: Rabbit
Dilution: WB 1：500-2000
Immunogen: Synthesized peptide derived from human ROM1 AA range: 163-213
Storage_stability: -20°C/1 year
Clonality: Polyclonal
Isotype: IgG
Concentration: 1 mg/ml
Human_gene_id: 6094
Human_swiss_prot_no: Q03395
Subcellular_location: Photoreceptor inner segment membrane ; Multi-pass membrane protein . Photoreceptor outer segment membrane ; Multi-pass membrane protein .
Background: This gene is a member of a photoreceptor-specific gene family and encodes an integral membrane protein found in the photoreceptor disk rim of the eye. This protein can form homodimers or can heterodimerize with another photoreceptor, retinal degeneration slow (RDS). It is essential for disk morphogenesis, and may also function as an adhesion molecule involved in the stabilization and compaction of outer segment disks or in the maintenance of the curvature of the rim. Certain defects in this gene have been associated with the degenerative eye disease retinitis pigmentosa. [provided by RefSeq, Jul 2008],
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