hnRNP C1 + C2 Antibody (9G1) - BSA Free

Novus Biologicals | Catalog # NBP3-26221

Recombinant Monoclonal Antibody
Novus Biologicals
100% Guarantee

Key Product Details

Species Reactivity

Human

Applications

Immunohistochemistry, Western Blot, ELISA, Flow Cytometry, Immunocytochemistry/ Immunofluorescence, Immunoprecipitation

Label

Unconjugated

Antibody Source

Recombinant Monoclonal Rabbit IgG Clone # 9G1 expressed in HEK293

Format

BSA Free
View all hnRNP C1 + C2 Primary Antibodies »

Product Specifications

Immunogen

A synthesized peptide derived from Human hnRNP C1 + C2 [UniProt P07910]

Clonality

Monoclonal

Host

Rabbit

Isotype

IgG

Scientific Data Images for hnRNP C1 + C2 Antibody (9G1) - BSA Free

hnRNP C1 + C2 Antibody (9G1)

Immunohistochemistry: hnRNP C1 + C2 Antibody (9G1) [NBP3-26221]

Immunohistochemistry: hnRNP C1 + C2 Antibody (9G1) [NBP3-26221] - NBP3-26221 diluted at 1:300 and staining in paraffin-embedded human braintissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.Secondary antibody only control: uses 1% BSA instead of primary antibody
hnRNP C1 + C2 Antibody (9G1)

Flow Cytometry: hnRNP C1 + C2 Antibody (9G1) [NBP3-26221]

Flow Cytometry: hnRNP C1 + C2 Antibody (9G1) [NBP3-26221] - Overlay Peak curve showing MCF7 cells stained with NBP3-26221 (red line) at 1:50. The cells were fixed in 4% formaldehyde and permeated by 0.2% TritonX-100. Then 10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (1ug/1*106cells) for 45min at 4℃. The secondary antibody used was FITC-conjugated Goat Anti-rabbit IgG (H+L) at 1:200 dilution for 35min at 4℃.Control antibody (green line) was Rabit IgG (1ug/1*106cells) used under the same conditions. Acquisition of >10,000 events was performed.
hnRNP C1 + C2 Antibody (9G1)

Immunocytochemistry/Immunofluorescence: hnRNP C1 + C2 Antibody (9G1) [NBP3-26221]

Immunocytochemistry/Immunofluorescence: hnRNP C1 + C2 Antibody (9G1) [NBP3-26221] - Staining of Hela cell with NBP3-26221 at 1:30, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG (H+L).
hnRNP C1 + C2 Antibody (9G1)

Immunocytochemistry/Immunofluorescence: hnRNP C1 + C2 Antibody (9G1) [NBP3-26221]

Immunocytochemistry/Immunofluorescence: hnRNP C1 + C2 Antibody (9G1) [NBP3-26221] - Staining of HepG2 cell with 5% goat serum, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG (H+L).
hnRNP C1 + C2 Antibody (9G1)

Immunocytochemistry/Immunofluorescence: hnRNP C1 + C2 Antibody (9G1) [NBP3-26221]

Immunocytochemistry/Immunofluorescence: hnRNP C1 + C2 Antibody (9G1) [NBP3-26221] - Staining of HepG2 cell with NBP3-26221 at 1:30, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG (H+L).
hnRNP C1 + C2 Antibody (9G1)

Immunohistochemistry: hnRNP C1 + C2 Antibody (9G1) [NBP3-26221]

Immunohistochemistry: hnRNP C1 + C2 Antibody (9G1) [NBP3-26221] - NBP3-26221 diluted at 1:300 and staining in paraffin-embedded human breast cancer performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.Secondary antibody only control: uses 1% BSA instead of primary antibody
hnRNP C1 + C2 Antibody (9G1)

Immunocytochemistry/Immunofluorescence: hnRNP C1 + C2 Antibody (9G1) [NBP3-26221]

Immunocytochemistry/Immunofluorescence: hnRNP C1 + C2 Antibody (9G1) [NBP3-26221] - Staining of Hela cell with 5% goat serum, counter-stained with DAPI. The cells were fixed in 4% formaldehyde and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG (H+L).
hnRNP C1 + C2 Antibody (9G1)

Immunohistochemistry: hnRNP C1 + C2 Antibody (9G1) [NBP3-26221]

Immunohistochemistry: hnRNP C1 + C2 Antibody (9G1) [NBP3-26221] - NBP3-26221 diluted at 1:300 and staining in paraffin-embedded human kidney tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.Secondary antibody only control: uses 1% BSA instead of primary antibody

Applications for hnRNP C1 + C2 Antibody (9G1) - BSA Free

Application
Recommended Usage

Immunocytochemistry/ Immunofluorescence

1:20-1:200

Immunohistochemistry

1:50-1:200

Immunoprecipitation

1:200-1:1000

Western Blot

1:500-1:5000

Flow Cytometry Panel Builder

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Flow Cytometry

Formulation, Preparation, and Storage

Purification

Affinity purified

Formulation

PBS, pH 7.4, 150mM NaCl, and 50% glycerol

Format

BSA Free

Preservative

0.02% Sodium Azide

Concentration

Please see the vial label for concentration. If unlisted please contact technical services.

Shipping

The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.

Stability & Storage

Store at -20 to -70C. Avoid freeze-thaw cycles.

Background: hnRNP C1 + C2

RNA polymerase II transcripts in the nucleus are in complex with several proteins called heterogeneous nuclear ribonucleoproteins (hnRNPs). These proteins are important in biological activities such as transcription, pre-mRNA processing, cytoplasmic mRNA translation, and turnover. hnRNPs can be isolated either by immunoprecipitation or by sucrose gradient fractionation of cell extracts. When this is performed, the hnRNPs are isolated (consisting of protein groups named A to U), and many of these protein groups consist of more than one isoform. The major steadystate proteins of the isolated hnRNP complex are the A1, A2, B1, B2, C1, and C2 with a range of molecular weight starting with 34 kDa up to 43 kDa. The hnRNP-C proteins have a single RNP motif RNA-binding domain (RBD) of 80 to 100 amino acid long. The hnRNP -C proteins preferentially bind to uridine-rich RNA sequences. Oligomerization of the protein through leucine rich regions in its C-terminal end is important for RNA binding.4 Although its physiological action is unknown, mutation of the hnRNPC gene causes a embryonic lethal phenotype.

Alternate Names

C1, C2, heterogeneous nuclear ribonucleoprotein C (C1/C2), heterogeneous nuclear ribonucleoproteins C1/C2, HNRNP, hnRNP C1/C2, hnRNPC, HNRPC, MGC104306, MGC105117, MGC117353, MGC131677, nuclear ribonucleoprotein particle C1 protein, nuclear ribonucleoprotein particle C2 protein, SNRPC

Gene Symbol

HNRNPC

Additional hnRNP C1 + C2 Products

Product Documents for hnRNP C1 + C2 Antibody (9G1) - BSA Free

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Product Specific Notices for hnRNP C1 + C2 Antibody (9G1) - BSA Free

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Protocols

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