PAX6 Monoclonal Antibody (1C8), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIMA515657-Each-of-1 | In Stock | ₹ 52,198.50 |
PIMA515657 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 52,198.50
GST (18%): ₹ 9,395.73
Total Price: ₹ 61,594.23
Antigen
PAX6
Classification
Monoclonal
Concentration
Conc. Not Determined
Formulation
ascites with 0.03% sodium azide
Gene Accession No.
P26367, P63015
Gene Symbols
PAX6
Immunogen
Purified recombinant fragment of human PAX6 expressed in E. Coli.
Regulatory Status
RUO
Gene ID (Entrez)
18508, 5080
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Applications
ELISA, Flow Cytometry, Western Blot
Clone
1C8
Conjugate
Unconjugated
Gene
PAX6
Gene Alias
1500038E17Rik; AEY11; AN; AN2; Aniridia; aniridia type II protein; D11S812E; Dey; Dickie's small eye; FVH1; Gsfaey11; Keratitis; MGC17209; MGDA; oculorhombin; paired box 6; paired box gene 6; Paired Box Gene-6; paired box homeotic gene 6; paired box homeotic gene-6; paired box protein Pax-6; Pax6; Pax-6; PAX6 protein; Sey; small eye; transcription factor; WAGR
Host Species
Mouse
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse
Product Type
Antibody
Isotype
IgG1
Related Products
Description
- MA5-15657 targets PAX6 in indirect ELISA, FACS and WB applications and shows reactivity with Human samples
- The MA5-15657 immunogen is purified recombinant fragment of human PAX6 expressed in E
- Coli
- <br>
- MA5-15657 detects PAX6 which has a predicted molecular weight of approximately 46kDa
- This gene encodes paired box gene 6, one of many human homologs of the Drosophila melanogaster gene prd
- In addition to the hallmark feature of this gene family, a conserved paired box domain, the encoded protein also contains a homeo box domain
- Both domains are known to bind DNA, and function as regulators of gene transcription
- This gene is expressed in the developing nervous system, and in developing eyes
- Mutations in this gene are known to cause ocular disorders such as aniridia and Peter's anomaly
- Alternatively spliced transcript variants encoding either the same or different isoform have been found for this gene.