ZC3H8 Polyclonal antibody

ZC3H8 Polyclonal Antibody for WB, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human

Applications

WB, ELISA

Conjugate

Unconjugated

Publications

1

Cat no : 26152-1-AP

Synonyms

Fliz1, ZC3H8, ZC3HDC8

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Validation Data Gallery

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  WB analysis of K-562 using 26152-1-AP

  K-562 cells were subjected to SDS PAGE followed by western blot with 26152-1-AP (ZC3H8 Antibody) at dilution of 1:2000 incubated at room temperature for 1.5 hours.

• 

  WB analysis using 26152-1-AP

  Various lysates were subjected to SDS PAGE followed by western blot with 26152-1-AP (ZC3H8 antibody) at dilution of 1:16000 incubated at room temperature for 1.5 hours.

• 

  WB analysis of PC-3 using 26152-1-AP

  PC-3 cells were subjected to SDS PAGE followed by western blot with 26152-1-AP (ZC3H8 Antibody) at dilution of 1:2000 incubated at room temperature for 1.5 hours.

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Tested Applications

• Positive WB detected in: K-562 cells, PC-3 cells

Recommended dilution

• Western Blot (WB): WB : 1:5000-1:50000

It is recommended that this reagent should be titrated in each testing system to obtain optimal results.

Sample-dependent, Check data in validation data gallery.

Published Applications

• WB: See 1 publications below

Product Information

The immunogen of 26152-1-AP is ZC3H8 Fusion Protein expressed in E. coli.

• Tested Reactivity: human
• Cited Reactivity: human
• Host / Isotype: Rabbit / IgG
• Class: Polyclonal
• Type: Antibody
• Immunogen: ZC3H8 fusion protein Ag23514
• Full Name: zinc finger CCCH-type containing 8
• Observed Molecular Weight: 35 kDa
• GenBank Accession Number: BC032001
• Gene Symbol: ZC3H8
• Gene ID (NCBI): 84524
• RRID: AB_2880406
• Conjugate: Unconjugated
• Form: Liquid
• Purification Method: Antigen affinity purification
• Storage Buffer: PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
• Storage Conditions: Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20^oC storage. 20ul sizes contain 0.1% BSA.

Publications

Species	Application	Title
human	WB	Am J Hum Genet; Mutations in SCNM1 cause orofaciodigital syndrome due to minor intron splicing defects affecting primary cilia; Authors - Asier Iturrate