Anti-PRPF4 Antibody

$99.00$319.00

Reactivity: Human
Applications: ELISA,WB,IHC
Conjugation: Various
Supplier: CUSABIO BIOTECH CO.

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Rabbit Anti-PRPF4 Antibody (CSB-PA018768ESR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

U4/U6 small nuclear ribonucleoprotein Prp4 Antibody,PRP4 homolog Antibody,hPrp4 Antibody,U4/U6 snRNP 60 kDa protein Antibody,WD splicing factor Prp4 Antibody,PRPF4 Antibody,PRP4 Antibody

More alternative names for the antibody
hPrp4 antibody|HPRP4P antibody|PRP4 antibody|PRP4 homolog antibody|PRP4 pre mRNA processing factor 4 homolog (yeast) antibody|PRP4/STK/WD splicing factor antibody|PRP4_HUMAN antibody|Prp4p antibody|PRPF4 antibody|RP70 antibody|SNRNP60 antibody|U4/U6 small nuclear ribonucleoprotein Prp4 antibody|U4/U6 snRNP 60 kDa protein antibody|WD splicing factor Prp4 antibody
Anti-PRPF4 antibody [EPR17207] – C-terminal (ab198998)
Close sc-163263|

Recommended applications: ELISA, WB, IHC

Recommended dilution: User optimized

Recommended protocols: check protocols

Name

Anti-PRPF4 Antibody

Catalogue No.

CSB-PA018768ESR2HU

Reactivity

Human

Immunogen

Recombinant human U4/U6 small nuclear ribonucleoprotein Prp4 protein (1-260AA)

Host

Rabbit

Applications

ELISA, WB, IHC

Recommended dilution

User optimized

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

58 kDa

Purification

Antigen Affinity Purified

Storage

Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.

Database links

Entrez Gene:9128( Human), Entrez Gene:70052( Mouse), Entrez Gene:298095( Rat), Omim:607795( Human), SwissProt:O43172( Human), SwissProt:Q9DAW6( Mouse), Unigene:744014( Human), Unigene:30660( Mouse)

Protein function

Participates in pre-mRNA splicing. Part of the U4/U5/U6 tri-snRNP complex, one of the building blocks of the spliceosome. .

Involvement in disease

Retinitis pigmentosa 70 (RP70) [MIM:615922]: A retinal dystrophy belonging to the group of pigmentary retinopathies. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein cellular localization

Nucleus speckle . Note=Colocalizes with spliceosomal snRNPs. .

Research area

All research areas>Transcription Regulators>PRPF
(View all antibody categories related to Transcription Regulators)

Note

AntibodyPlus provides antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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