Mouse Anti-SDR9C7 Recombinant Antibody (CBXS-4865) (CBMAB-S2088-CQ)

Name: Mouse Anti-SDR9C7 Recombinant Antibody (CBXS-4865)
SKU: CBMAB-S2088-CQ
Rating: 5 (1 reviews)

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Datasheet

SDS

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Datasheet Target Q & As Review & reward Protocols Associated Products

Basic Information

Host Animal

Mouse

Clone

CBXS-4865

Application

Immunogen

Recombinant full length human SDR9C7 (NP_683695)

Specificity

Human

Antibody Isotype

IgG1

Clonality

Monoclonal

Application Notes

The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Format

Liquid

Buffer

PBS, pH 7.3, 1% BSA, 50% glycerol

Preservative

0.02% sodium azide

Storage

Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

More Infomation

Target

Full Name

Short Chain Dehydrogenase/Reductase Family 9C Member 7

Introduction

This gene encodes a protein with similarity to the short-chain dehydrogenase/reductase (SDR) family but has not been shown to have retinoid or dehydrogenase activities.

Entrez Gene ID

121214

UniProt ID

Q8NEX9

Alternative Names

Short Chain Dehydrogenase/Reductase Family 9C Member 7; Orphan Short-Chain Dehydrogenase/Reductase; RDH-S; SDR-O; RDHS; SDRO; Short Chain Dehydrogenase/Reductase Family 9C, Member 7;

Function

Displays weak conversion of all-trans-retinal to all-trans-retinol in the presence of NADH. Has apparently no steroid dehydrogenase activity.

Biological Process

Biological Process retinol metabolic processManual Assertion Based On ExperimentIBA:GO_Central
Biological Process steroid metabolic processManual Assertion Based On ExperimentIBA:GO_Central

Cellular Location

Cytoplasm
Granular distribution in the whole cell.

Involvement in disease

Ichthyosis, congenital, autosomal recessive 13 (ARCI13):
A form of autosomal recessive congenital ichthyosis, a disorder of keratinization with abnormal differentiation and desquamation of the epidermis, resulting in abnormal skin scaling over the whole body. The main skin phenotypes are lamellar ichthyosis (LI) and non-bullous congenital ichthyosiform erythroderma (NCIE), although phenotypic overlap within the same patient or among patients from the same family can occur. Lamellar ichthyosis is a condition often associated with an embedment in a collodion-like membrane at birth; skin scales later develop, covering the entire body surface. Non-bullous congenital ichthyosiform erythroderma characterized by fine whitish scaling on an erythrodermal background; larger brownish scales are present on the buttocks, neck and legs.

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Please try the standard protocols which include: protocols, troubleshooting and guide.

Enzyme-linked Immunosorbent Assay (ELISA)
Flow Cytometry
Immunofluorescence (IF)
Immunohistochemistry (IHC)
Immunoprecipitation (IP)
Western Blot (WB)
Enzyme Linked Immunospot (ELISpot)
Proteogenomic
Other Protocols

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Isotype control

For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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