7121469
Human/Mouse/Rat RBBP4 Antibody, R&D Systems™
Mouse Monoclonal Antibody has been used in 1 publication
Manufacturer: Fischer Scientific
The price for this product is unavailable. Please request a quote
Antigen
RBBP4/RbAp48
Dilution
Western Blot 0.5 ug/mL, Immunohistochemistry 5 ug/mL
Classification
Monoclonal
Host Species
Mouse
Target Species
Human, Mouse, Rat
Gene Accession No.
9028
Gene ID (Entrez)
5928
Isotype
IgG2b
Purification Method
Protein A or G purified from hybridoma culture supernatant
Content And Storage
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.12 months from date of receipt, -20 to -70 degreesC as supplied. 1 month, 2 to 8 degreesC under sterile conditions after reconstitution. 6 months, -20 to -70 degreesC under sterile conditions after reconstitution.
Clone
968701
Applications
Western Blot, Immunohistochemistry
Conjugate
Unconjugated
Regulatory Status
RUO
Formulation
Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. *Small pack size (SP) is supplied as a 0.2 μm filtered solution in PBS.
Gene Alias
CAF-1 p48, CAF-1 subunit C, CAF-1C, CAF-I p48, Chromatin assembly factor 1 subunit C, Chromatin assembly factor I p48 subunit, chromatin assembly factor/CAF-1 p48 subunit, histone-binding protein RBBP4, MSI1 protein homolog, Nucleosome-remodeling factor subunit RBAP48, NURF55, RbAp48, RBBP-4, retinoblastoma binding protein 4, Retinoblastoma-binding protein 4CAF-I 48 kDa subunit, Retinoblastoma-binding protein p48
Immunogen
E. coli-derived recombinant human RBBP-4 Ala2-Ser425 Accession # 09028
Primary or Secondary
Primary
Reconstitution
Reconstitute at 0.5 mg/mL in sterile PBS.
Test Specificity
Detects human RBBP-4 in direct ELISAs and Western blots.
Related Products
Description
- RBBP4/RbAp48 Monoclonal specifically detects RBBP4/RbAp48 in Human, Mouse, Rat samples
- It is validated for Western Blot, Immunohistochemistry.
Compare Similar Items
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Antigen: RBBP4/RbAp48
Dilution: Western Blot 0.5 ug/mL, Immunohistochemistry 5 ug/mL
Classification: Monoclonal
Host Species: Mouse
Target Species: Human, Mouse, Rat
Gene Accession No.: 9028
Gene ID (Entrez): 5928
Isotype: IgG2b
Purification Method: Protein A or G purified from hybridoma culture supernatant
Content And Storage: Use a manual defrost freezer and avoid repeated freeze-thaw cycles.12 months from date of receipt, -20 to -70 degreesC as supplied. 1 month, 2 to 8 degreesC under sterile conditions after reconstitution. 6 months, -20 to -70 degreesC under sterile conditions after reconstitution.
Clone: 968701
Applications: Western Blot, Immunohistochemistry
Conjugate: Unconjugated
Regulatory Status: RUO
Formulation: Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. *Small pack size (SP) is supplied as a 0.2 μm filtered solution in PBS.
Gene Alias: CAF-1 p48, CAF-1 subunit C, CAF-1C, CAF-I p48, Chromatin assembly factor 1 subunit C, Chromatin assembly factor I p48 subunit, chromatin assembly factor/CAF-1 p48 subunit, histone-binding protein RBBP4, MSI1 protein homolog, Nucleosome-remodeling factor subunit RBAP48, NURF55, RbAp48, RBBP-4, retinoblastoma binding protein 4, Retinoblastoma-binding protein 4CAF-I 48 kDa subunit, Retinoblastoma-binding protein p48
Immunogen: E. coli-derived recombinant human RBBP-4 Ala2-Ser425 Accession # 09028
Primary or Secondary: Primary
Reconstitution: Reconstitute at 0.5 mg/mL in sterile PBS.
Test Specificity: Detects human RBBP-4 in direct ELISAs and Western blots.
Antigen:
RBBP4/RbAp48
Dilution:
Western Blot 0.5 ug/mL, Immunohistochemistry 5 ug/mL
Classification:
Monoclonal
Host Species:
Mouse
Target Species:
Human, Mouse, Rat
Gene Accession No.:
9028
Gene ID (Entrez):
5928
Isotype:
IgG2b
Purification Method:
Protein A or G purified from hybridoma culture supernatant
Content And Storage:
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.12 months from date of receipt, -20 to -70 degreesC as supplied. 1 month, 2 to 8 degreesC under sterile conditions after reconstitution. 6 months, -20 to -70 degreesC under sterile conditions after reconstitution.
Clone:
968701
Applications:
Western Blot, Immunohistochemistry
Conjugate:
Unconjugated
Regulatory Status:
RUO
Formulation:
Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. *Small pack size (SP) is supplied as a 0.2 μm filtered solution in PBS.
Gene Alias:
CAF-1 p48, CAF-1 subunit C, CAF-1C, CAF-I p48, Chromatin assembly factor 1 subunit C, Chromatin assembly factor I p48 subunit, chromatin assembly factor/CAF-1 p48 subunit, histone-binding protein RBBP4, MSI1 protein homolog, Nucleosome-remodeling factor subunit RBAP48, NURF55, RbAp48, RBBP-4, retinoblastoma binding protein 4, Retinoblastoma-binding protein 4CAF-I 48 kDa subunit, Retinoblastoma-binding protein p48
Immunogen:
E. coli-derived recombinant human RBBP-4 Ala2-Ser425 Accession # 09028
Primary or Secondary:
Primary
Reconstitution:
Reconstitute at 0.5 mg/mL in sterile PBS.
Test Specificity:
Detects human RBBP-4 in direct ELISAs and Western blots.
Antigen: PTH
Dilution: Flow Cytometry 0.5 - 1 ug/million cells, Immunocytochemistry/Immunofluorescence 0.5 - 1 ug/ml, Immunohistochemistry-Paraffin 0.5 - 1.0 ug/ml, CyTOF-ready
Classification: Monoclonal
Host Species: Rabbit
Target Species: Human
Gene Accession No.: __
Gene ID (Entrez): 5741
Isotype: IgG κ
Purification Method: Protein A or G purified
Content And Storage: Store at -20 to -80C. Avoid freeze-thaw cycles.
Clone: PTH/1717R
Applications: Flow Cytometry, Immunocytochemistry, Immunofluorescence, Immunohistochemistry (Paraffin), CyTOF
Conjugate: Unconjugated
Regulatory Status: RUO
Formulation: PBS with No Preservative
Gene Alias: Parathormone, Parathyrin, parathyroid hormone, parathyroid hormone 1, PTH1
Immunogen: Recombinant human PTH protein N-terminal fragment (exact sequence is proprietary)
Primary or Secondary: Primary
Reconstitution: __
Test Specificity: __
Antigen:
PTH
Dilution:
Flow Cytometry 0.5 - 1 ug/million cells, Immunocytochemistry/Immunofluorescence 0.5 - 1 ug/ml, Immunohistochemistry-Paraffin 0.5 - 1.0 ug/ml, CyTOF-ready
Classification:
Monoclonal
Host Species:
Rabbit
Target Species:
Human
Gene Accession No.:
__
Gene ID (Entrez):
5741
Isotype:
IgG κ
Purification Method:
Protein A or G purified
Content And Storage:
Store at -20 to -80C. Avoid freeze-thaw cycles.
Clone:
PTH/1717R
Applications:
Flow Cytometry, Immunocytochemistry, Immunofluorescence, Immunohistochemistry (Paraffin), CyTOF
Conjugate:
Unconjugated
Regulatory Status:
RUO
Formulation:
PBS with No Preservative
Gene Alias:
Parathormone, Parathyrin, parathyroid hormone, parathyroid hormone 1, PTH1
Immunogen:
Recombinant human PTH protein N-terminal fragment (exact sequence is proprietary)
Primary or Secondary:
Primary
Reconstitution:
__
Test Specificity:
__
Antigen: PTH
Dilution: Flow Cytometry 0.5 - 1 ug/million cells, Immunocytochemistry/Immunofluorescence 0.5 - 1 ug/ml, Immunohistochemistry-Paraffin 0.5 - 1.0 ug/ml, CyTOF-ready
Classification: Monoclonal
Host Species: Mouse
Target Species: Human
Gene Accession No.: __
Gene ID (Entrez): 5741
Isotype: IgG2b κ
Purification Method: Protein A or G purified
Content And Storage: Store at -20 to -80C. Avoid freeze-thaw cycles.
Clone: SPM604
Applications: Flow Cytometry, Immunocytochemistry, Immunofluorescence, Immunohistochemistry (Paraffin), CyTOF
Conjugate: Unconjugated
Regulatory Status: RUO
Formulation: PBS with No Preservative
Gene Alias: Parathormone, Parathyrin, parathyroid hormone, parathyroid hormone 1, PTH1
Immunogen: A synthetic peptide from the N-terminal of human PTH polypeptide.
Primary or Secondary: Primary
Reconstitution: __
Test Specificity: Epitope of this MAb maps in the N-terminus of PTH, a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion.It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism.
Antigen:
PTH
Dilution:
Flow Cytometry 0.5 - 1 ug/million cells, Immunocytochemistry/Immunofluorescence 0.5 - 1 ug/ml, Immunohistochemistry-Paraffin 0.5 - 1.0 ug/ml, CyTOF-ready
Classification:
Monoclonal
Host Species:
Mouse
Target Species:
Human
Gene Accession No.:
__
Gene ID (Entrez):
5741
Isotype:
IgG2b κ
Purification Method:
Protein A or G purified
Content And Storage:
Store at -20 to -80C. Avoid freeze-thaw cycles.
Clone:
SPM604
Applications:
Flow Cytometry, Immunocytochemistry, Immunofluorescence, Immunohistochemistry (Paraffin), CyTOF
Conjugate:
Unconjugated
Regulatory Status:
RUO
Formulation:
PBS with No Preservative
Gene Alias:
Parathormone, Parathyrin, parathyroid hormone, parathyroid hormone 1, PTH1
Immunogen:
A synthetic peptide from the N-terminal of human PTH polypeptide.
Primary or Secondary:
Primary
Reconstitution:
__
Test Specificity:
Epitope of this MAb maps in the N-terminus of PTH, a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion.It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism.
Antigen: PTH
Dilution: Flow Cytometry 0.5 - 1 ug/million cells, Immunocytochemistry/Immunofluorescence 0.5 - 1 ug/ml, Immunohistochemistry-Paraffin 0.5 - 1.0 ug/ml, CyTOF-ready
Classification: Monoclonal
Host Species: Mouse
Target Species: Human
Gene Accession No.: __
Gene ID (Entrez): 5741
Isotype: IgG2b κ
Purification Method: Protein A or G purified
Content And Storage: Store at -20 to -80C. Avoid freeze-thaw cycles.
Clone: PTH/911
Applications: Flow Cytometry, Immunocytochemistry, Immunofluorescence, Immunohistochemistry (Paraffin), CyTOF
Conjugate: Unconjugated
Regulatory Status: RUO
Formulation: PBS with No Preservative
Gene Alias: Parathormone, Parathyrin, parathyroid hormone, parathyroid hormone 1, PTH1
Immunogen: A synthetic peptide from the N-terminal of human PTH polypeptide.
Primary or Secondary: Primary
Reconstitution: __
Test Specificity: Epitope of this MAb maps in the N-terminus of PTH, a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion.It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism.
Antigen:
PTH
Dilution:
Flow Cytometry 0.5 - 1 ug/million cells, Immunocytochemistry/Immunofluorescence 0.5 - 1 ug/ml, Immunohistochemistry-Paraffin 0.5 - 1.0 ug/ml, CyTOF-ready
Classification:
Monoclonal
Host Species:
Mouse
Target Species:
Human
Gene Accession No.:
__
Gene ID (Entrez):
5741
Isotype:
IgG2b κ
Purification Method:
Protein A or G purified
Content And Storage:
Store at -20 to -80C. Avoid freeze-thaw cycles.
Clone:
PTH/911
Applications:
Flow Cytometry, Immunocytochemistry, Immunofluorescence, Immunohistochemistry (Paraffin), CyTOF
Conjugate:
Unconjugated
Regulatory Status:
RUO
Formulation:
PBS with No Preservative
Gene Alias:
Parathormone, Parathyrin, parathyroid hormone, parathyroid hormone 1, PTH1
Immunogen:
A synthetic peptide from the N-terminal of human PTH polypeptide.
Primary or Secondary:
Primary
Reconstitution:
__
Test Specificity:
Epitope of this MAb maps in the N-terminus of PTH, a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2+ levels by dissolving the salts in bone and preventing their renal excretion.It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism.