LSBio
PathPlus™ AVPR1B Antibody (C-Terminus)

Anti-AVPR1B antibody IHC of human pancreas islet of Langerhans. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval.

PathPlus™ AVPR1B Antibody (C-Terminus)

Primary AntibodyLSBio Guarantee
Antibody:Rabbit Polyclonal
Applications:Immunohistochemistry (general)
Reactivity:Human
Format:Liquid
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$403.00each
Catalog Number: LS-A3737-50

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Overview

Description
AVPR1B antibody LS-A3737 is an unconjugated rabbit polyclonal antibody to human AVPR1B (C-Terminus). Validated for IHC. Cited in 1 publication.
Application
IHC
Reactivity
Hu
Intended Use
Research Use Only
Guarantees
This product carries the LSBio 100% Guarantee.
Category
Antibodies > Primary Antibodies > Polyclonal Antibodies
Alternative Names
AVPR1B | AVPR3 | V1bR | AVPR V1b | AVPR V3 | V1b receptor | V1b vasopressin receptor | Vasopressin V1b receptor | Vasopressin V3 receptor | VPR3 | Vasopressin V1B Receptor
Recommended Dilution: IHC-P
2 - 7 µg/ml
UniProt Number
P47901
SwissProt
P47901

Target

Target
AVPR1B
Antigen Species
Human
Specificity
Human AVPR1B. BLAST analysis of the peptide immunogen showed no homology with other human proteins.
Epitope
Human AVPR1B. BLAST analysis of the peptide immunogen showed no homology with other human proteins.
Gene Name
AVPR1B

Antibody

Host Species
Rabbit
Clonality
Polyclonal

Immunogen

Immunogen
Synthetic 19 amino acid peptide from C-Terminus of human AVPR1B. Percent identity with other species by BLAST analysis: Human, Gorilla, Gibbon (100%); Monkey, Marmoset (89%); Bovine (84%).
Immunogen Type
Synthetic Peptide (Linear)

Format

Conjugate/Label
Unconjugated
Format
Liquid
Formulation
PBS, 0.1% Sodium Azide
Concentration
1 mg/mL
Animal Free
No
Carrier-Free
Yes
Preservative
Yes
Purification Method
Affinity Purified

Storage & Handling

Storage Conditions
Aliquot and store undiluted at -20°C or below for up to 1 year. Can be stored undiluted at 4°C for up to 1 month. Avoid freeze-thaw cycles.
Recommended Storage Buffer
PBS
Impact of USP8 Gene Mutations on Protein Deregulation in Cushing Disease. Isabel Weigand, Lisanne Knobloch, Jörg Flitsch, Wolfgang Saeger, Camelia M Monoranu, Kerstin Höfner, Sabine Herterich, Roman Rotermund, Cristina L Ronchi, Michael Buchfelder, Markus Glatzel, Christian Hagel, Martin Fassnacht, Timo Deutschbein, Silviu Sbiera. The Journal of clinical endocrinology and metabolism. 2019 July;104:2535-2546. PubMed: 30844069

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