Inhibin Binding Protein (INHBP) ELISA Kits

INHBP encodes a member of the immunoglobulin-like domain-containing superfamily. Additionally we are shipping Inhibin Binding Protein Antibodies (57) and Inhibin Binding Protein Proteins (11) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
INHBP 3547 Q8N6C5
INHBP 209268 Q7TQA1
INHBP 302822 Q925N6
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Top Inhibin Binding Protein ELISA Kits at

Showing 10 out of 25 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Delivery Price Details
Rat 15.63 pg/mL n/a   96 Tests 13 to 16 Days
Mouse 0.469 ng/mL 0.781-50 ng/mL Diagramm of the ELISA kit to detect Mouse 1 NHBPwith the optical density on the x-axis and the concentration on the y-axis. Typical standard curve 96 Tests 12 to 14 Days
Human 0.39 ng/mL 1.56 ng/mL - 100 ng/mL 96 Tests 15 to 17 Days
Guinea Pig 0.1 ng/mL 2.5-50 ng/mL   96 Tests 15 to 18 Days
Rabbit 0.1 ng/mL 2.5-50 ng/mL   96 Tests 15 to 18 Days
Monkey 1.0 ng/mL 5.0-100 ng/mL   96 Tests 15 to 18 Days
  96 Tests 15 to 18 Days
Dog 0.1 ng/mL 2.5-50 ng/mL   96 Tests 15 to 18 Days
  96 Tests 15 to 18 Days
  96 Tests 15 to 18 Days

More ELISA Kits for Inhibin Binding Protein Interaction Partners

Human Inhibin Binding Protein (INHBP) interaction partners

  1. A novel mutation (c.2713C>T, p.Q905X) of the IGSF1 gene was identified that causes congenital central hypothyroidism in a Japanese family. The findings further expand the clinical heterogeneity of this entity.

  2. We identified a novel insertion mutation in the IGSF1 gene and further delineated the phenotype of the IGSF1-deficiency syndrome. Our findings indicate a possible association between an IGSF1 mutation and neurological phenotypes.

  3. Individuals with identical IGSF1 deletions can exhibit variable pituitary hormone deficiencies, of which overt TSH deficiency is the most consistent feature

  4. IGSF1 Deficiency is associated with X-linked IGSF1 deficiency syndrome.

  5. Adult male patients with IGSF1 deficiency exhibit mild deficits in attentional control on formal testing.

  6. This case suggests that more attention should be paid to intrauterine growth and birth history when patients are suspected of having an IGSF1 mutation

  7. There is insufficient evidence to conclude that the three observed VUCSs in IGSF1 are associated with CDGP, making it unlikely that IGSF1 mutations are a prevalent cause of CDGP.

  8. Immunohistochemistry showed increased IGSF1 staining in the GH-producing tumor from the patient with the IGSF1 p.N604T variant compared with a GH-producing adenoma from a patient negative for any IGSF1 variants and with normal control pituitary tissue.

  9. Data suggest male subjects with IGSF1 deficiency syndrome exhibit X-linked congenital/central hypothyroidism, delayed puberty, macro-orchidism, hypoprolactinemia, metabolic syndrome, and transient partial growth hormone deficiency. [CASE REPORTS]

  10. Our findings provide additional genetic evidence that loss-of-function mutations in IGSF1 cause an X-linked form of C-CH and variable prolactin deficiency.

  11. Using exome and candidate gene sequencing, 8 distinct mutations and 2 deletions in IGSF1 were identified in males from 11 unrelated families with central hypothyroidism, testicular enlargement and variably low prolactin concentrations.

  12. IgSF1 is processed through sequential proteolysis by signal peptidase and signal peptide peptidase

Mouse (Murine) Inhibin Binding Protein (INHBP) interaction partners

  1. Contrary to earlier predictions, neither the murine nor rat IGSF1-2 is secreted from heterologous or homologous cells. In addition, neither protein associates with the plasma membrane. Rather, IGSF1-2 appears to be retained in the endoplasmic reticulum.

  2. Igsf1-deficient males exhibit normal serum TSH levels as well as normal numbers of TSH-expressing thyrotropes. However, pituitary expression of the TSH subunit genes and TSH protein content are reduced, as is expression of the receptor for thyrotropin-releasing hormone (TRH

Inhibin Binding Protein (INHBP) Antigen Profile

Antigen Summary

This gene encodes a member of the immunoglobulin-like domain-containing superfamily. Proteins in this superfamily contain varying numbers of immunoglobulin-like domains and are thought to participate in the regulation of interactions between cells. Multiple transcript variants encoding different isoforms have been found for this gene.

Gene names and symbols associated with INHBP

  • immunoglobulin superfamily member 1 (IGSF1) antibody
  • immunoglobulin superfamily, member 1 (Igsf1) antibody
  • inhibin binding protein (LOC443288) antibody
  • 5330413N23 antibody
  • 5530402E03 antibody
  • AI747649 antibody
  • CHTE antibody
  • IGCD1 antibody
  • IGDC1 antibody
  • Inhbp antibody
  • InhBP/p120 antibody
  • mKIAA0364 antibody
  • p120 antibody
  • PGSF2 antibody

Protein level used designations for INHBP

immunoglobulin superfamily member 1 , immunoglobulin-like domain-containing protein 1 , inhibin-binding protein , pituitary gland-specific factor 2 , betaglycan and inhibin binding protein , inhBP , inhibin binding protein

481051 Canis lupus familiaris
100058129 Equus caballus
100157227 Sus scrofa
3547 Homo sapiens
100125775 Bos taurus
209268 Mus musculus
302822 Rattus norvegicus
443288 Ovis aries
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