PIPA533580

GHSR Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA533580-Each-of-1 In Stock ₹ 46,502.50

PIPA533580 - Each of 1

₹ 46,502.50

In Stock

Quantity

1

Base Price: ₹ 46,502.50

GST (18%): ₹ 8,370.45

Total Price: ₹ 54,872.95

Antigen

GHSR

Classification

Polyclonal

Conjugate

Unconjugated

Gene

Ghsr

Gene Alias

C530020I22Rik; GHDP; GH-releasing peptide receptor; Ghrelin receptor; GHRP; Ghrp receptor; GHS receptor; GHSR; GHS-R; G-protein coupled receptor; growth hormone secretagogue receptor; growth hormone secretagogue receptor type 1

Host Species

Rabbit

Purification Method

Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

2693

Content And Storage

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

Form

Liquid

Applications

Immunohistochemistry (Paraffin)

Concentration

1 mg/mL

Formulation

PBS with 0.1% sodium azide

Gene Accession No.

Q92847

Gene Symbols

Ghsr

Immunogen

Synthetic 16 amino acid peptide from internal region of human Ghrelin Receptor.

Quantity

50 μg

Primary or Secondary

Primary

Target Species

Human, Non-human Primate

Product Type

Antibody

Isotype

IgG

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Description

  • Percent identity with other species by BLAST analysis: Human, Gorilla, Gibbon, Baboon, Monkey, Marmoset (100%)
  • Growth hormone secretagogue receptor 1a (GHSR) is a member of the G-protein coupled receptor family
  • GHSR may play a role in energy homeostasis and regulation of body weight
  • Two identified transcript variants are expressed in several tissues and are evolutionary conserved in fish and swine
  • One transcript, 1a, excises an intron and encodes the functional protein; this protein is the receptor for the Ghrelin ligand and defines a neuroendocrine pathway for growth hormone release
  • The second transcript (1b) retains the intron and does not function as a receptor for Ghrelin; however, it may function to attenuate activity of isoform 1a
  • Mutations to the gene can cause isolated partial growth hormone deficiency.