C19orf44 Polyclonal antibody

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• C19orf44 Polyclonal antibody (21503-1-AP)

C19orf44 Polyclonal Antibody for WB, ELISA

Cat No. 21503-1-AP Copied!

Publications (1)

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Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat

Applications

WB, IF, ELISA

Synonyms

chromosome 19 open reading frame 44

• 

  WB analysis of L02 using 21503-1-AP

  L02 cells were subjected to SDS PAGE followed by western blot with 21503-1-AP (C19orf44 antibody) at dilution of 1:600 incubated at room temperature for 1.5 hours.

  This validation data has been generated in-house and reviewed by Proteintech scientists. Find out more on our antibody validation policy
• 

  WB analysis of rat brain using 21503-1-AP

  rat brain tissue were subjected to SDS PAGE followed by western blot with 21503-1-AP (C19orf44 antibody) at dilution of 1:600 incubated at room temperature for 1.5 hours.

  This validation data has been generated in-house and reviewed by Proteintech scientists. Find out more on our antibody validation policy
• 

  WB analysis of mouse liver using 21503-1-AP

  mouse liver tissue were subjected to SDS PAGE followed by western blot with 21503-1-AP (C19orf44 antibody) at dilution of 1:500 incubated at room temperature for 1.5 hours.

  This validation data has been generated in-house and reviewed by Proteintech scientists. Find out more on our antibody validation policy
• 

  WB analysis of mouse liver using 21503-1-AP

  mouse liver tissue were subjected to SDS PAGE followed by western blot with 21503-1-AP (C19orf44 antibody) at dilution of 1:600 incubated at room temperature for 1.5 hours.

  This validation data has been generated in-house and reviewed by Proteintech scientists. Find out more on our antibody validation policy

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Tested Applications

• Positive WB detected in: L02 cells, mouse liver tissue, rat brain tissue

Recommended dilution

• Western Blot (WB): WB : 1:500-1:1000

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.

Product Information

21503-1-AP targets C19orf44 in WB, IF, ELISA applications and shows reactivity with human, mouse, rat samples.

• Tested Reactivity: human, mouse, rat
• Cited Reactivity: human
• Host / Isotype: Rabbit / IgG
• Class: Polyclonal
• Type: Antibody
• Immunogen:

  CatNo: Ag15960

  Product name: Recombinant human C19orf44 protein

  Source: e coli.-derived, PGEX-4T

  Tag: GST

  Domain: 1-350 aa of BC027869

  Sequence: MASARKASRPMRDVFGDFSDVSLEDSTMEEIRNFQISRNLTKIAPGHSRFLKRNQTLDEKHLLLKENPVLGSGPRLASCRPPTTASRIRANAALMKLAQLETRIMNRKLQRNLSDTESDSMTADAGLPKRADRILSGGALELASQNTDKTSQNQARELPVTENNAQNAKVSRFLKKKQAPVENISPEAPAGKERTLQTPKQKEPARTFDSPDSDEEEMKVLLGSLMDSSREKNTNQGFSSANVSEEEERKLFSVPSQLRAFTVPSVELSSAKPSQTSHLPTSLAADRTLHSTRSRADYPQSHVSSDTASHTPSVSITGAFSNSVSLKMGHVKLVSSPGRSEAETVDEPVS

• Full Name: chromosome 19 open reading frame 44
• Calculated Molecular Weight: 618 aa, 66 kDa
• Observed Molecular Weight: 66-71 kDa
• GenBank Accession Number: BC027869
• Gene Symbol: C19orf44
• Gene ID (NCBI): 84167
• RRID: AB_2878871
• Conjugate: Unconjugated
• Form: Liquid
• Purification Method: Antigen affinity purification
• UNIPROT ID: Q9H6X5
• 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

What published studies show

The C19orf44 Polyclonal antibody (Cat# 21503-1-AP) has 1 citation to date. It was cited in Genet Med (Impact Factor 6.2) in a 2025 study by Miriam Ehrenberg et al., which investigated biallelic null variants in C19orf44 causing a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophy. The research field is medical genetics and ophthalmology, specifically retinal degenerative disease. The antibody was used for immunofluorescence (IF) in human samples.

Automatically generated from the 1 publication citations by Able AI.

• Human
• Mouse
• Rat
• Monkey
• Pig

Species	Application	Title
human	IF	Genet Med; Biallelic null variants in C19orf44 cause a unique late onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophy; Authors - Miriam Ehrenberg