Search results for Retinol Dehydrogenase 12 (RDH12) Antibody

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Retinol Dehydrogenase 12 (RDH12) Antibody Brand Logo
ID: BAB018660678

Retinol Dehydrogenase 12 (RDH12) Antibody, Abbexa, abx145096

Retinol Dehydrogenase 12 (RDH12) Antibody is a Rabbit Polyclonal against Retinol Dehydrogenase 12 (RDH12). The protein encoded by this gene is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. The encoded enzyme also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 13 and Retinitis Pigmentosa 53.

Host

Rabbit

Reactivity

Human

Applications

ELISA, WB, IHC

Conjugation

Unconjugated

Retinol Dehydrogenase 12 (RDH12) Antibody Brand Logo
ID: BAB517155079

Retinol Dehydrogenase 12 (RDH12) Antibody, Abbexa, abx321053

Retinol Dehydrogenase 12 (RDH12) Antibody is a Rabbit Polyclonal against Retinol Dehydrogenase 12 (RDH12). The protein encoded by this gene is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. The encoded enzyme also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 13 and Retinitis Pigmentosa 53.

Host

Rabbit

Reactivity

Human

Applications

ELISA, IHC

Conjugation

Unconjugated

Retinol Dehydrogenase 12 (RDH12) Antibody Brand Logo
ID: BAB500453215

Retinol Dehydrogenase 12 (RDH12) Antibody, Abbexa, abx301572

Retinol Dehydrogenase 12 (RDH12) Antibody is a Rabbit Polyclonal against Retinol Dehydrogenase 12 (RDH12). The protein encoded by this gene is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. The encoded enzyme also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 13 and Retinitis Pigmentosa 53.

Host

Rabbit

Reactivity

Human

Applications

ELISA, IHC

Conjugation

Unconjugated

Retinol Dehydrogenase 12 (RDH12) Antibody (FITC) Brand Logo
ID: BAB859259756

Retinol Dehydrogenase 12 (RDH12) Antibody (FITC), Abbexa, abx309613

Retinol Dehydrogenase 12 (RDH12) Antibody (FITC) is a Rabbit Polyclonal against Retinol Dehydrogenase 12 (RDH12) conjugated to FITC. The protein encoded by this gene is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. The encoded enzyme also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 13 and Retinitis Pigmentosa 53.

Host

Rabbit

Reactivity

Human

Applications

Conjugation

FITC

Retinol Dehydrogenase 12 (RDH12) Antibody (Biotin) Brand Logo
ID: BAB043482551

Retinol Dehydrogenase 12 (RDH12) Antibody (Biotin), Abbexa, abx309614

Retinol Dehydrogenase 12 (RDH12) Antibody (Biotin) is a Rabbit Polyclonal against Retinol Dehydrogenase 12 (RDH12) conjugated to Biotin. The protein encoded by this gene is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. The encoded enzyme also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 13 and Retinitis Pigmentosa 53.

Host

Rabbit

Reactivity

Human

Applications

ELISA

Conjugation

Biotin

Retinol Dehydrogenase 12 (RDH12) Antibody (HRP) Brand Logo
ID: BAB770344754

Retinol Dehydrogenase 12 (RDH12) Antibody (HRP), Abbexa, abx309612

Retinol Dehydrogenase 12 (RDH12) Antibody (HRP) is a Rabbit Polyclonal against Retinol Dehydrogenase 12 (RDH12) conjugated to HRP. The protein encoded by this gene is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. The encoded enzyme also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 13 and Retinitis Pigmentosa 53.

Host

Rabbit

Reactivity

Human

Applications

ELISA

Conjugation

HRP

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