OPLAH antibody (AA 1119-1288)

Catalog No. ABIN6145037

The Rabbit Polyclonal anti-OPLAH antibody has been validated for WB. It is suitable to detect OPLAH in samples from Human.

Quick Overview for OPLAH antibody (AA 1119-1288) (ABIN6145037)

Target: OPLAH (5-Oxoprolinase (ATP-Hydrolysing) (OPLAH))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This OPLAH antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-OPLAH Antibody

Binding Specificity: AA 1119-1288

Sequence: TVAGGAGAGP SWHGRSGVHS HMTNTRITDP EILESRYPVI LRRFELRRGS GGRGRFRGGD GVTRELLFRE EALLSVLTER RAFRPYGLHG GEPGARGLNL LIRKNGRTVN LGGKTSVTVY PGDVFCLHTP GGGGYGDPED PAPPPGSPPQ ALAFPEHGSV YEYRRAQEAV

Cross-Reactivity: Human, Mouse, Rat

Characteristics: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1119-1288 of human OPLAH (NP_060040.1).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000

Comment:

HIGH QUALITY

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Preservative: Sodium azide

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

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for OPLAH

Target: OPLAH (5-Oxoprolinase (ATP-Hydrolysing) (OPLAH))

Alternative Name: OPLAH

Background: The protein encoded by this gene acts as a homodimer, using ATP hydrolysis to catalyze the conversion of 5-oxo-L-proline to L-glutamate. Defects in this gene are a cause of 5-oxoprolinase deficiency (OPLAHD).,OPLAH,5-Opase,OPLA,OPLAHD,Signal Transduction,Endocrine & Metabolism,Amino acid metabolism,OPLAH

Molecular Weight: 137 kDa

Gene ID: 26873

UniProt: O14841