CABP2 Antibody

Code CSB-PA873608LA01HU
Size US$166
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  • Immunofluorescent analysis of HepG2 cells using CSB-PA873608LA01HU at dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L)

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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) CABP2 Polyclonal antibody
Uniprot No.
Target Names
CABP2
Alternative Names
CaBP2 antibody; CABP2_HUMAN antibody; Calcium-binding protein 2 antibody
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Recombinant Human Calcium-binding protein 2 protein (6-172AA)
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated

The CABP2 Antibody (Product code: CSB-PA873608LA01HU) is Non-conjugated. For CABP2 Antibody with conjugates, please check the following table.

Available Conjugates
Conjugate Product Code Product Name Application
HRP CSB-PA873608LB01HU CABP2 Antibody, HRP conjugated ELISA
FITC CSB-PA873608LC01HU CABP2 Antibody, FITC conjugated
Biotin CSB-PA873608LD01HU CABP2 Antibody, Biotin conjugated ELISA
Clonality
Polyclonal
Isotype
IgG
Purification Method
>95%, Protein G purified
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Tested Applications
ELISA, IF
Recommended Dilution
Application Recommended Dilution
IF 1:50-1:200
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

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Target Background

Function
Required for sound encoding at inner hair cells (IHCs) synapses, likely via inhibition of the inactivation of voltage-gated calcium channel of type 1.3 (Cav1.3) in the IHCs. Required for the normal transfer of light signals through the retina.
Gene References into Functions
  1. Genetic defects in CABP2 cause moderate-to-severe sensorineural hearing impairment. PMID: 22981119
Involvement in disease
Deafness, autosomal recessive, 93 (DFNB93)
Subcellular Location
Cytoplasm, perinuclear region. Cell membrane; Lipid-anchor; Cytoplasmic side. Golgi apparatus.
Tissue Specificity
Retina.
Database Links

HGNC: 1385

OMIM: 607314

KEGG: hsa:51475

STRING: 9606.ENSP00000294288

UniGene: Hs.278984

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7505 Fannin St., Ste 610, Room 7 (CUBIO Innovation Center), Houston, TX 77054, USA
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