SCAPER Polyclonal antibody
SCAPER Polyclonal Antibody for IHC, ELISA
Host / Isotype
Rabbit / IgG
Reactivity
human, mouse
Applications
IF, IHC, ELISA
Conjugate
Unconjugated
Cat no : 16994-1-AP
Synonyms
Validation Data Gallery
Tested Applications
Positive IHC detected in | mouse testis tissue, human testis tissue Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0 |
Recommended dilution
Application | Dilution |
---|---|
Immunohistochemistry (IHC) | IHC : 1:50-1:500 |
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
IHC | See 1 publications below |
IF | See 1 publications below |
Product Information
The immunogen of 16994-1-AP is SCAPER Fusion Protein expressed in E. coli.
Tested Reactivity | human, mouse |
Cited Reactivity | mouse |
Host / Isotype | Rabbit / IgG |
Class | Polyclonal |
Type | Antibody |
Immunogen | SCAPER fusion protein Ag10679 |
Full Name | S-phase cyclin A-associated protein in the ER |
Calculated Molecular Weight | 292 aa, 32 kDa |
GenBank Accession Number | BC015212 |
Gene Symbol | SCAPER |
Gene ID (NCBI) | 49855 |
RRID | AB_2878339 |
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 -20oC storage. 20ul sizes contain 0.1% BSA. |
Background Information
SCAPER, also named as KIAA1454 and ZNF291, is a CCNA2/CDK2 regulatory protein that transiently maintains CCNA2 in the cytoplasm.
Protocols
Product Specific Protocols | |
---|---|
IHC protocol for SCAPER antibody 16994-1-AP | Download protocol |
Standard Protocols | |
---|---|
Click here to view our Standard Protocols |
Publications
Species | Application | Title |
---|---|---|
J Med Genet Mutations in SCAPER cause autosomal recessive retinitis pigmentosa with intellectual disability. | ||