Products for Research Use Only

Connexin 26 Rabbit Polyclonal Antibody

CAT: 0013-GTR17721717-01Size: 50 μLDry Ice: NoHazardous: No
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CAT#:0013-GTR17721717-01Size:50 μL
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Description
Connexin 26 Rabbit Polyclonal Antibody
Product Name Alternative
BAPS; CX26; DFNA3; DFNA3A; DFNB1; DFNB1A; HID; KID; NSRD1; PPK; Cnx26; Cxne; Gjb-2; CXN-26; CXB2_HUMAN; GJB2; Connexin-26 (Cx26) ; CXB2_MOUSE; CXB2_RAT; gap junction protein beta 2; gap junction protein, beta 2, 26kD (connexin 26) ; gap junction protein, beta 2, 26kDa (connexin 26) ; gap junction protein, beta 2, 26kDa; connexin 26
UniProt
P29033
Reactivity
Human
Immunogen
KLH conjugated synthetic peptide derived from human Connexin-26 (81-180/226aa)
Target
GJB2
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Cell Signaling, Gap junctions, Neuroscience
Purification
Affinity purified by Protein A
Concentration
1mg/ml
Dilution
WB=1:500-2000, IHC-P=1:100-500, IHC-F=1:100-500, IF=1:100-500, ELISA=1:5000-10000
Form
Liquid
Molecular Weight
26 kDa
Storage Conditions
Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Notes
For research use only.
Prediction Reactivity
Bovine, Canine, Equine, Gallus, Human, Mouse, Porcine, Rabbit, Rat, Sheep
Tested Applications
ELISA, IF, IHC-Fr, IHC-P, WB
Host or Source
Rabbit
Preservative
0.01M TBS (pH7.4) with 1% rAlbumin, 0.02% Proclin300 and 50% Glycerol.
Isotype
IgG

UniProtKB · P29033

Gap junction beta-2 protein

CXB2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P29033
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
GJB2
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
Q508A5, Q508A6, Q5YLL0, Q5YLL1, Q5YLL4, Q6IPV5, Q86U88, Q96AK0, Q9H536, Q9NNY4
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Ligand

CalciumMetal-binding

Cellular component

Cell junctionCell membraneGap junctionMembrane

Disease

DeafnessDisease variantEctodermal dysplasiaIchthyosisNon-syndromic deafnessPalmoplantar keratoderma

PTM

Disulfide bond

Biological process

Hearing

Domain

TransmembraneTransmembrane helix