Use Able AI chat for product recommendations
  • Featured Product
  • KD/KO Validated

CSPP1 Polyclonal antibody

CSPP1 Polyclonal Antibody for WB, IF/ICC, IP, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat

Applications

WB, IHC, IF/ICC, IP, ELISA

Centrosome and spindle pole-associated protein 1, CSPP

Formulation:  PBS, Azide, Glycerol
PBS, Azide, Glycerol
Conjugate:  Unconjugated
Size/Concentration: 
SKU: 

-/ -

Freight/Packing: -

Quantity

Please visit your regions distributor:

Able AI
Able AI
What's the best dilution for CSPP1 in ?

Tested Applications

Positive WB detected inJurkat cells, HEK-293 cells, HeLa cells, mouse testis tissue, rat testis tissue
Positive IP detected inJurkat cells
Positive IF/ICC detected inHeLa cells

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:500-1:1000
Immunoprecipitation (IP)IP : 0.5-4.0 ug for 1.0-3.0 mg of total protein lysate
Immunofluorescence (IF)/ICCIF/ICC : 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.

Product Information

11931-1-AP targets CSPP1 in WB, IHC, IF/ICC, IP, ELISA applications and shows reactivity with human, mouse, rat samples.

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

CatNo: Ag2521

Product name: Recombinant human CSPP1 protein

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

Tag: GST

Domain: 1-208 aa of BC029445

Sequence: MADNLDEFIEEQKARLAEDKAELESDPPYMEMKGKLSAKLSENSKILISMAKENIPPNSQQTRGSLGIDYGLSLPLGEDYERKKHKLKEELRQDYRRYLTQERLKLERNKEYNQFLRGKEESSEKFRQVEKSTEPKSQRNKKPIGQVKPDLTSQIQTSCENSEGPRKDVLTPSEAYEELLNQRRLEEDRYRQLDDEIELRNRRIIKSK

Predict reactive species
Full Name centrosome and spindle pole associated protein 1
Calculated Molecular Weight 141 kDa
Observed Molecular Weight 141 kDa
GenBank Accession NumberBC029445
Gene Symbol CSPP1
Gene ID (NCBI) 79848
RRIDAB_2087897
Conjugate Unconjugated
FormLiquid
Purification MethodAntigen affinity purification
UNIPROT IDQ1MSJ5
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol, pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA.

Background Information

CSPP1 interacts with centrosomes and microtubules and plays a role in cell-cycle progression and spindle organization. CSPP1 is required for their common C-terminal domain to interact with Nephrocystin 8 (NPHP8/RPGRIP1L) and to form a ternary complex with NPHP8 and NPHP4, and for ciliogenesis in hTERT-RPE1 cells in vitro and are expressed in ciliated renal, retinal, and respiratory cells in vivo

Protocols

Product Specific Protocols
IF protocol for CSPP1 antibody 11931-1-APDownload protocol
IP protocol for CSPP1 antibody 11931-1-APDownload protocol
WB protocol for CSPP1 antibody 11931-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

What published studies show

The anti-CSPP1 monoclonal antibody (Cat# 11931-1-AP) has accumulated 13 citations across journals including Science Advances, Methods in Cell Biology, British Journal of Cancer, American Journal of Human Genetics, Cell Reports, PLoS Biology, EMBO Reports, Molecular Biology of the Cell, PLoS ONE, and Cilia. Associated research fields include ciliopathies (Joubert syndrome), primary cilia biology, Hedgehog signaling, cell migration, mitotic spindle organization, centriolar satellite stability, and breast cancer subtyping.

SpeciesApplicationTitle
humanIF

Sci Adv

eIF2A regulates cell migration in a translation-independent manner.

Authors - Jennifer Jungfleisch
mouseIF

Methods Cell Biol

Fixation methods and immunolabeling for cilia proteins in ciliary and extraciliary locations

Authors - Kiet Hua
humanIHC,IF

Br J Cancer

Nuclear CSPP1 expression defined subtypes of basal-like breast cancer.

Authors - J Sternemalm
  • KD Validated
humanWB,IF

Am J Hum Genet

Mutations in CSPP1 Cause Primary Cilia Abnormalities and Joubert Syndrome with or without Jeune Asphyxiating Thoracic Dystrophy.

Authors - Karina Tuz
humanWB,IF

Am J Hum Genet

Mutations in CSPP1 Lead to Classical Joubert Syndrome.

Authors - Naiara Akizu
humanWB

Cell Rep

A CEP104-CSPP1 Complex Is Required for Formation of Primary Cilia Competent in Hedgehog Signaling.

Authors - Kari-Anne M Frikstad
  • KO Validated
Loading...
||
New chat

Able™

正在加载,请稍候...