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BLNK Antibody (N-term)Purified Rabbit Polyclonal Antibody (Pab)

Country
United States
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Ordering Information
Catalog # Size Availability Price  
AP13433a 0.1 mg 400 ul In Stock $ 255.00 Add to cart
AP13433a-ev20 20 ug 100 ul In Stock $ 95.00 Add to cart
  • Specification
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BLNK Antibody (N-term) - Product info

ApplicationWB
  • Applications Legend:
  • W=Western Blotting
  • IP=Immunoprecipitation
  • IHC-P=Immunohistochemistry (Paraffin)
  • IF-IC=Immunofluorescence (Immunocytochemistry)
  • F=Flow Cytometry
Primary AccessionQ8WV28
Other AccessionQ4KM52, Q9QUN3, NP_037446.1, NP_001107566.1
ReactivityHuman
PredictedMouse, Rat
Concentration0.25 mg/ml
IsotypeRabbit Ig
Calculated MW50466 Da

BLNK Antibody (N-term) - Additional info

Gene ID 29760
Other Names
BLNK; BASH; SLP65; B-cell linker protein; B-cell adapter containing a SH2 domain protein; B-cell adapter containing a Src homology 2 domain protein; Cytoplasmic adapter protein; Src homology 2 domain-containing leukocyte protein of 65 kDa
Target/Specificity
This BLNK antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 56-82 amino acids from the N-terminal region of human BLNK.
Dilution
WB~~1:50~100
Format
Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.
Storage
Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Precautions
BLNK Antibody (N-term) is for research use only and not for use in diagnostic or therapeutic procedures.

BLNK Antibody (N-term) - Protein Information

Name BLNK
Synonyms BASH, SLP65
Function
Functions as a central linker protein, downstream of the B-cell receptor (BCR), bridging the SYK kinase to a multitude of signaling pathways and regulating biological outcomes of B-cell function and development. Plays a role in the activation of ERK/EPHB2, MAP kinase p38 and JNK. Modulates AP1 activation Important for the activation of NF-kappa-B and NFAT. Plays an important role in BCR-mediated PLCG1 and PLCG2 activation and Ca(2+) mobilization and is required for trafficking of the BCR to late endosomes. However, does not seem to be required for pre-BCR- mediated activation of MAP kinase and phosphatidyl-inositol 3 (PI3) kinase signaling. May be required for the RAC1-JNK pathway Plays a critical role in orchestrating the pro-B cell to pre-B cell transition. May play an important role in BCR-induced B-cell apoptosis
Cellular Location
Cytoplasm. Cell membrane. Note=BCR activation results in the translocation to membrane fraction
Tissue Location
Expressed in B-cell lineage and fibroblast cell lines (at protein level). Highest levels of expression in the spleen, with lower levels in the liver, kidney, pancreas, small intestines and colon

BLNK Antibody (N-term) - Related products

AP13433a: BLNK Antibody (N-term)

AP6502c: BLNK Antibody (Center)

RI10603: BLNK predesign siRNA

DC04766: Human BLNK cDNA Clone

LY10908a: BLNK Over-expression Lysate

BP6502c: BLNK Antibody (Center) Blocking Peptide

AJ1101a: BLNK Antibody

AF1158a: BLNK / SLP-65 Antibody

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BACKGROUND

This gene encodes a cytoplasmic linker or adaptor protein that plays a critical role in B cell development. This protein bridges B cell receptor-associated kinase activation with downstream signaling pathways, thereby affecting various biological functions. The phosphorylation of five tyrosine residues is necessary for this protein to nucleate distinct signaling effectors following B cell receptor activation. Mutations in this gene cause hypoglobulinemia and absent B cells, a disease in which the pro- to pre-B-cell transition is developmentally blocked. Deficiency in this protein has also been shown in some cases of pre-B acute lymphoblastic leukemia. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

REFERENCES

Rose, J.E., et al. Mol. Med. 16 (7-8), 247-253 (2010) : Davila, S., et al. Genes Immun. 11(3):232-238(2010) Oellerich, T., et al. Mol. Cell Proteomics 8(7):1738-1750(2009) Imamura, Y., et al. J. Biol. Chem. 284(15):9804-9813(2009) Li, H., et al. PLoS ONE 4 (7), E6410 (2009) :