223

TPI1 Antibody | 26-284

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SKU:
223-26-284-GEN
$2,467.50

Description

TPI1 Antibody | 26-284 | Gentaur UK, US & Europe Distribution

Host: Rabbit

Reactivity: Human

Homology: N/A

Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human TPI1.

Research Area: Cancer

Tested Application: E, WB

Application: TPI1 antibody can be used for detection of TPI1 by ELISA at 1:1562500. TPI1 antibody can be used for detection of TPI1 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50, 000 - 100, 000.

Specificiy: N/A

Positive Control 1: Cat. No. 1211 - HepG2 Cell Lysate

Positive Control 2: N/A

Positive Control 3: N/A

Positive Control 4: N/A

Positive Control 5: N/A

Positive Control 6: N/A

Molecular Weight: 27 kDa

Validation: N/A

Isoform: N/A

Purification: Antibody is purified by peptide affinity chromatography method.

Clonality: Polyclonal

Clone: N/A

Isotype: N/A

Conjugate: Unconjugated

Physical State: Liquid

Buffer: Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.

Concentration: batch dependent

Storage Condition: For short periods of storage (days) store at 4˚C. For longer periods of storage, store TPI1 antibody at -20˚C. As with any antibody avoid repeat freeze-thaw cycles.

Alternate Name: TPI1, MGC88108, TPI, TIM, TPID, HEL-S-49

User Note: Optimal dilutions for each application to be determined by the researcher.

BACKGROUND: TPI1 belongs to the triosephosphate isomerase family. Defects in TPI1 are the cause of triosephosphate isomerase deficiency (TPI deficiency) . TPI deficiency is an autosomal recessive disorder. It is the most severe clinical disorder of glycolysis. It is associated with neonatal jaundice, chronic hemolytic anemia, progressive neuromuscular dysfunction, cardiomyopathy and increased susceptibility to infection.

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Additional Information

Size:
100 uL
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