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anti-Chromosome 2 Open Reading Frame 71 (C2orf71) Antibodies

The protein encoded by C2orf71 is highly expressed in photoreceptors and may associate with the primary cilium of the outer segment. Additionally we are shipping and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
C2orf71 388939 A6NGG8
C2orf71    
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Top anti-C2orf71 Antibodies at antibodies-online.com

Showing 10 out of 16 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Human Rabbit Un-conjugated WB WB Suggested Anti-C2orf71 AntibodyTitration: 1.0 µg/mL  Positive Control: Fetal kidney 100 μL Log in to see 2 to 3 Days
$289.00
Details
Human Rabbit Un-conjugated WB   50 μg Log in to see 8 to 10 Days
$551.83
Details
Human Rabbit Alexa Fluor 555 IF (p)   100 μL Log in to see 14 to 21 Days
$357.50
Details
Human Rabbit Alexa Fluor 647 IF (p)   100 μL Log in to see 14 to 21 Days
$357.50
Details
Human Rabbit FITC IF (p)   100 μL Log in to see 14 to 21 Days
$357.50
Details
Human Rabbit Biotin IHC (p), WB   100 μL Log in to see 14 to 21 Days
$357.50
Details
Human Rabbit Alexa Fluor 350 IF (p)   100 μL Log in to see 14 to 21 Days
$357.50
Details
Human Rabbit Alexa Fluor 488 IF (p)   100 μL Log in to see 14 to 21 Days
$357.50
Details
Human Rabbit Alexa Fluor 594 IF (p)   100 μL Log in to see 14 to 21 Days
$357.50
Details
Human Rabbit HRP IHC (p), WB   100 μL Log in to see 14 to 21 Days
$379.50
Details

C2orf71 Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality Conjugate
Human , ,


, , , , , , , , , , ,
Rat (Rattus) ,


, , , , , , , , , , ,

More Antibodies against C2orf71 Interaction Partners

Human Chromosome 2 Open Reading Frame 71 (C2orf71) interaction partners

  1. A homozygous nonsense CEP250 (show CEP250 Antibodies) mutation, in combination with a heterozygous C2orf71 nonsense mutation, causes an atypical form of Usher syndrome, characterised by early-onset sensorineural hearing loss and a relatively mild retinitis pigmentosa.

  2. Novel C2orf71 mutations account for approximately 1% of cases in a large French arRP cohort.

  3. C2ORF71 is a highly polymorphic gene (average heterozygosity of coding region in controls: 2.118 x 10(-3)) with many rare variants that confound mutation detection.

  4. Mutations in C2orf71 cause autosomal-recessive retinitis pigmentosa.

  5. Discovery and functional analysis of a retinitis pigmentosa gene, C2orf71, are reported.

C2orf71 Antigen Profile

Protein Summary

The protein encoded by this gene is highly expressed in photoreceptors and may associate with the primary cilium of the outer segment. The encoded protein appears to undergo post-translational lipid modification. Nonsense and missense variants of this gene appear to cause a recessive form of retinitis pigmentosa.

Gene names and symbols associated with C2orf71

  • hypothetical LOC517881 (C11H2orf71) antibody
  • chromosome 2 open reading frame 71 (C2orf71) antibody

Protein level used designations for C2orf71

hypothetical LOC517881 , uncharacterized protein C2orf71

GENE ID SPECIES
517881 Bos taurus
388939 Homo sapiens
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