DHRS13 antibody (AA 101-200)

Catalog No. ABIN1387987

This Rabbit Polyclonal antibody specifically detects DHRS13 in WB and ELISA. It exhibits reactivity toward Mouse.

Quick Overview for DHRS13 antibody (AA 101-200) (ABIN1387987)

Target: DHRS13 (Dehydrogenase/reductase (SDR Family) Member 13 (DHRS13))

Reactivity: Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This DHRS13 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-DHRS13 Antibody

Binding Specificity: AA 101-200

Cross-Reactivity: Mouse

Predicted Reactivity: Human,Rat,Cow,Sheep,Horse

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human DHRS13

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
ELISA 1:500-1000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Expiry Date: 12 months

Target Details for DHRS13

Target: DHRS13 (Dehydrogenase/reductase (SDR Family) Member 13 (DHRS13))

Alternative Name: Dhrs13

Background:

Synonyms: Dehydrogenase/reductase SDR family member 13, Dehydrogenase/reductase SDR family member 13, DHRS 13, MGC23280, OTTHUMP00000163522, SDR7C5, Short chain dehydrogenase/reductase family 7C member 5, DHR13_HUMAN.

Background: DHRS13 (dehydrogenase/reductase SDR family member 13), also known as UNQ419/PRO853, is a 377 amino acid secreted protein belonging to the short-chain dehydrogenases/reductases (SDR) family. DHRS13 is presumed to function as an oxidoreductase and is phosphorylated, potentially by ATM or ATR, upon DNA damage. DHRS13 exists as two isoforms produced by alternative splicing events. The gene encoding DHRS13 maps to human chromosome 17, which comprises over 2.5 % of the human genome and encodes over 1,200 genes. Neurofibromatosis, dysregulated Schwann cell growth, Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease are associated with chromosome 17.

Gene ID: 147015