Product: Substance P Antibody
Catalog: DF6541
Description: Rabbit polyclonal antibody to Substance P
Application: WB IHC IF/ICC
Reactivity: Human, Mouse, Rat
Prediction: Bovine, Sheep, Rabbit, Dog
Mol.Wt.: 15kDa; 15kD(Calculated).
Uniprot: P20366
RRID: AB_2838503

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 100ul $280 In stock
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Product Info

Source:
Rabbit
Application:
WB 1:500-1:2000, IHC 1:50-1:200, IF/ICC 1:100-1:500
*The optimal dilutions should be determined by the end user.
*Tips:

WB: For western blot detection of denatured protein samples. IHC: For immunohistochemical detection of paraffin sections (IHC-p) or frozen sections (IHC-f) of tissue samples. IF/ICC: For immunofluorescence detection of cell samples. ELISA(peptide): For ELISA detection of antigenic peptide.

Reactivity:
Human,Mouse,Rat
Prediction:
Bovine(86%), Sheep(100%), Rabbit(100%), Dog(100%)
Clonality:
Polyclonal
Specificity:
Substance P Antibody detects endogenous levels of total Substance P.
RRID:
AB_2838503
Cite Format: Affinity Biosciences Cat# DF6541, RRID:AB_2838503.
Conjugate:
Unconjugated.
Purification:
The antiserum was purified by peptide affinity chromatography using SulfoLink™ Coupling Resin (Thermo Fisher Scientific).
Storage:
Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
Alias:

Fold/Unfold

C-terminal-flanking peptide; neurokinin A; neurokinin alpha; NKA; NKNA; PPT; preprotachykinin; protachykinin; protachykinin-1; SubstanceP; TAC1; TAC2; Tachykinin 1; Tachykinin precursor 1; Tachykinin1; TKN1_HUMAN; SP;

Immunogens

Immunogen:
Uniprot:
Gene(ID):
Description:
This gene encodes four products of the tachykinin peptide hormone family, substance P and neurokinin A, as well as the related peptides, neuropeptide K and neuropeptide gamma. These hormones are thought to function as neurotransmitters which interact with nerve receptors and smooth muscle cells. They are known to induce behavioral responses and function as vasodilators and secretagogues. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Sequence:
MKILVALAVFFLVSTQLFAEEIGANDDLNYWSDWYDSDQIKEELPEPFEHLLQRIARRPKPQQFFGLMGKRDADSSIEKQVALLKALYGHGQISHKRHKTDSFVGLMGKRALNSVAYERSAMQNYERRR

Predictions

Predictions:

Score>80(red) has high confidence and is suggested to be used for WB detection. *The prediction model is mainly based on the alignment of immunogen sequences, the results are for reference only, not as the basis of quality assurance.

Species
Results
Score
Sheep
100
Dog
100
Rabbit
100
Bovine
86
Pig
0
Horse
0
Xenopus
0
Zebrafish
0
Chicken
0
Model Confidence:
High(score>80) Medium(80>score>50) Low(score<50) No confidence

Research Backgrounds

Function:

Tachykinins are active peptides which excite neurons, evoke behavioral responses, are potent vasodilators and secretagogues, and contract (directly or indirectly) many smooth muscles.

PTMs:

The substance P form is cleaved at Pro-59 by the prolyl endopeptidase FAP (seprase) activity (in vitro).

Subcellular Location:

Secreted.

Extracellular region or secreted Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi apparatus Nucleus Mitochondrion Manual annotation Automatic computational assertionSubcellular location
Family&Domains:

Belongs to the tachykinin family.

References

1). Substance P Mediates Estrogen Modulation Proinflammatory Cytokines Release in Intervertebral Disc. INFLAMMATION, 2021 (PubMed: 32965648) [IF=4.5]

Application: IHC    Species: mouse    Sample: NP cells

Fig. 1.| Effects of ERT on SP and its receptor NK1R in NP cells. After OVX, the staining intensity of NK1R (a–c) and SP (d–f) in NP cells significantly increased compared with the sham group. While OVX+E2 could reverse these changes. Bar represents 50 μm.

2). Electroacupuncture Stimulation Alleviates Inflammatory Pain in Male Rats by Suppressing Oxidative Stress. Physiological research, 2023 (PubMed: 38015764) [IF=1.9]

Application: WB    Species: Rat    Sample: C6 glioma cells

Fig. 5 ROS induced proinflammatory cytokine and CIP-related substance production in C6 glioma cells. C6 cells were treated with t-BOOH (50 μM) and PBN (100 μM) for 24 h. (A): ROS were assayed by a DCFHA probe (A1: CON; C2: t-BOOH; C3: PBN); (B–D): cytokines were measured by ELISA kits; (E): expression of p-p38, p-ERK, p-p65, SP, TRPV1 and TRPV4 was determined by western blotting. GAPDH was used as a loading control. t-BOOH: tert-butyl hydroperoxide; PBN: phenyl-N-tert-butylnitrone (ROS scavenger); data are represented as the mean ± standard deviation; n=4 per group; ## P

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Affinity Biosciences tests all products strictly. Citations are provided as a resource for additional applications that have not been validated by Affinity Biosciences. Please choose the appropriate format for each application and consult Materials and Methods sections for additional details about the use of any product in these publications.

For Research Use Only.
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