Connexin 47 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA5113633-Each-of-1 | In Stock | ₹ 46,502.50 |
PIPA5113633 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
Connexin 47
Classification
Polyclonal
Conjugate
Unconjugated
Gene
GJC2
Gene Alias
B230382L12Rik; connexin 47 type A; connexin 47 type C; connexin 47 type D; connexin-46.6; Connexin-47; CX46.6; Cx47; CXG2; gap junction alpha-12 protein; Gap junction gamma-2 protein; gap junction membrane channel protein alpha 12; gap junction protein gamma 2; gap junction protein, alpha 12; gap junction protein, chi 2; gap junction protein, gamma 2; gap junction protein, gamma 2, 47kDa; GJA12; Gjc2; HLD2; LMPH1C; PMLDAR; SPG44
Host Species
Rabbit
Purification Method
Affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
57165
Content And Storage
-20° C, Avoid Freeze/Thaw Cycles
Form
Liquid
Applications
Immunohistochemistry (Paraffin), Western Blot
Concentration
0.5 mg/mL
Formulation
PBS with 2% sucrose and 0.09% sodium azide
Gene Accession No.
Q5T442
Gene Symbols
GJC2
Immunogen
Synthetic peptide directed towards the middle region of human GJC2
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Immunogen sequence: APASRTGSAT SAGTVGEQGR PGTHERPGAK PRAGSEKGSA SSRDGKTTVW For short term use, store at 2-8°C up to 1 week
- For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles
- Predicted homology: Human: 100%; Rabbit: 100% This gene encodes a member of the gap junction protein family
- The gap junction proteins are membrane-spanning proteins that assemble to form gap junction channels that facilitate the transfer of ions and small molecules between cells
- According to sequence similarities at the nucleotide and amino acid levels, the gap junction proteins are divided into two categories, alpha and beta
- Mutations in this gene cause X-linked Charcot-Marie-Tooth disease, an inherited peripheral neuropathy
- Alternatively spliced transcript variants encoding the same protein have been found for this gene.